Gene ontology: date: 05:12:2007 15:33 Revision: 5.589
For annotation versions, see below.
Locate OMIM disorder using this index
A B C D E F G H I J K L M N O P R S T U V W X Y Z 2 3


A
OMIM disorder(s)OMIM_idComparisonGraphMouseHumanRatWormFlyDictyChickenZfinRiceTairYeastPombePfalc
ABCD syndrome600501Graph: ABCD syndromeMouseHumanRatXXXXXXXXXX
ACTH deficiency201400Graph: ACTH deficiencyMouseHumanRatXFlyXXXXXXXX
ADULT syndrome103285Graph: ADULT syndromeMouseHumanRatXXXXXXXXXX
AICA-ribosiduria due to ATIC deficiency608688Graph: AICA-ribosiduria due to ATIC deficiencyXHumanRatXXXXXXXYeastXX
AIDS, rapid progression to609423Graph: AIDS, rapid progression toMouseHumanRatXXXXXXXXXX
ARC syndrome208085Graph: ARC syndromeXXXXXXXXXXYeastXX
Abetalipoproteinemia200100Graph: AbetalipoproteinemiaMouseXXXXXXZfinXXXXX
Acampomelic campolelic dysplasia114290Graph: Acampomelic campolelic dysplasiaMouseHumanXXXXXZfinXXXXX
Achalasia-addisonianism-alacrimia syndrome231550Graph: Achalasia-addisonianism-alacrimia syndromeXHumanXXXXXXXXXXX
Acheiropody200500Graph: AcheiropodyMouseXXXXXXXXXXXX
Achondrogenesis Ib600972Graph: Achondrogenesis IbXHumanRatXXXXXXXXXX
Achondrogenesis-hypochondrogenesis, type II200610Graph: Achondrogenesis-hypochondrogenesis, type IIMouseHumanRatXXXXXXXXXX
Achondroplasia100800Graph: AchondroplasiaMouseHumanXWormXXXXXXXXX
Achromatopsia-2216900Graph: Achromatopsia-2MouseHumanXXXXXXXXXXX
Achromatopsia-3262300Graph: Achromatopsia-3MouseHumanXXXXXXXXXXX
Acrocallosal syndrome200990Graph: Acrocallosal syndromeMouseHumanRatXFlyXXXXXYeastXX
Acrocapitofemoral dysplasia607778Graph: Acrocapitofemoral dysplasiaMouseXXWormXXXXXXXXX
Acrodermatitis enteropathica201100Graph: Acrodermatitis enteropathicaMouseXXXXXXXXXXXX
Acrokeratosis verruciformis101900Graph: Acrokeratosis verruciformisMouseHumanRatWormXXXXXXXXX
Acromegaly102200Graph: AcromegalyMouseXRatWormXXXXXXXXX
Acromesomelic dysplasia, Hunter-Thompson type201250Graph: Acromesomelic dysplasia, Hunter-Thompson typeMouseHumanXXXXXXXXXXX
Acromesomelic dysplasia, Maroteaux type602875Graph: Acromesomelic dysplasia, Maroteaux typeMouseHumanXXXXXXXXXXX
Acyl-CoA dehydrogenase, medium chain, deficiency of201450Graph: Acyl-CoA dehydrogenase, medium chain, deficiency ofMouseHumanRatXXXXXXXXXX
Acyl-CoA dehydrogenase, short-chain, deficiency of201470Graph: Acyl-CoA dehydrogenase, short-chain, deficiency ofMouseHumanRatXXXXXXXXXX
Adenocarcinoma of lung, response to tyrosine kinase inhibitor in211980Graph: Adenocarcinoma of lung, response to tyrosine kinase inhibitor inMouseHumanRatWormXDictyXXXXYeastXX
Adenocarcinoma of lung, somatic211980Graph: Adenocarcinoma of lung, somaticMouseHumanRatWormXDictyXXXXYeastXX
Adenocarcinoma, ovarian, somatic604370Graph: Adenocarcinoma, ovarian, somaticMouseHumanRatWormXDictyXXXXXXX
Adenomas, multiple colorectal608456Graph: Adenomas, multiple colorectalMouseHumanRatXXXXXXXXXX
Adenomas, salivary gland pleomorphic181030Graph: Adenomas, salivary gland pleomorphicXHumanXXXXXXXTairXXX
Adenylosuccinase deficiency103050Graph: Adenylosuccinase deficiencyXHumanXXXXXXXXYeastXX
Adrenal cortical carcinoma202300Graph: Adrenal cortical carcinomaMouseHumanRatXXXXXXXXXX
Adrenal hyperplasia, congenital, due to combined P450C17 and P450C21 deficiency201750Graph: Adrenal hyperplasia, congenital, due to combined P450C17 and P450C21 deficiencyMouseHumanXXXXXXXXYeastXX
Adrenal hypoplasia, congenital, with hypogonadotropic hypogonadism300200Graph: Adrenal hypoplasia, congenital, with hypogonadotropic hypogonadismMouseXXXXXXXXXXXX
Adrenocorticotropic hormone deficiency201400Graph: Adrenocorticotropic hormone deficiencyMouseHumanRatXFlyXXXXXXXX
Adrenoleukodystrophy300100Graph: AdrenoleukodystrophyXHumanXXXXXXXXYeastXX
Adrenoleukodystrophy, neonatal202370Graph: Adrenoleukodystrophy, neonatalMouseHumanXWormXXXXXXYeastXX
Adrenomyeloneuropathy300100Graph: AdrenomyeloneuropathyXHumanXXXXXXXXYeastXX
Adult i phenotype with congenital cataract110800Graph: Adult i phenotype with congenital cataractMouseHumanXXXXXXXXXXX
Adult i phenotype without cataract110800Graph: Adult i phenotype without cataractMouseHumanXXXXXXXXXXX
Advanced sleep phase syndrome, familial604348Graph: Advanced sleep phase syndrome, familialMouseHumanRatXXXXXXXXXX
Afibrinogenemia, congenital202400Graph: Afibrinogenemia, congenitalXHumanRatXXXXXXXXXX
Agammaglobulinemia601495Graph: AgammaglobulinemiaMouseHumanXXXXXXXXXXX
Agammaglobulinemia, autosomal recessive601495Graph: Agammaglobulinemia, autosomal recessiveMouseHumanXXXXXXXXXXX
Agammaglobulinemia, non-Bruton type601495Graph: Agammaglobulinemia, non-Bruton typeMouseHumanXXXXXXXXXXX
Agenesis of the corpus callosum with peripheral neuropathy218000Graph: Agenesis of the corpus callosum with peripheral neuropathyMouseHumanXXXXXXXXXXX
Alagille syndrome118450Graph: Alagille syndromeMouseHumanRatXXXXZfinXXXXX
Albinism, brown203290Graph: Albinism, brownMouseXXXXXXXXXXXX
Albinism, oculocutaneous, type IA203100Graph: Albinism, oculocutaneous, type IAMouseHumanXXXXXXXXXXX
Albinism, oculocutaneous, type IB606952Graph: Albinism, oculocutaneous, type IBMouseHumanXXXXXXXXXXX
Albinism, rufous278400Graph: Albinism, rufousMouseXXXXXXXXXXXX
Aldosteronism, glucocorticoid-remediable103900Graph: Aldosteronism, glucocorticoid-remediableXHumanRatXXXXXXXXXX
Alexander disease203450Graph: Alexander diseaseMouseHumanRatWormXXXZfinXXXXX
Alkaptonuria203500Graph: AlkaptonuriaXHumanXXXXXXXXXXX
Allan-Herndon-Dudley syndrome300523Graph: Allan-Herndon-Dudley syndromeXHumanXXXXXXXXYeastXX
Alopecia universalis203655Graph: Alopecia universalisXXXXXXXXXXXXX
Alpers syndrome203700Graph: Alpers syndromeMouseHumanRatXXXXXXXYeastXX
Alpha-methylacetoacetic aciduria203750Graph: Alpha-methylacetoacetic aciduriaMouseHumanRatXXXXXXXYeastXX
Alpha-thalassemia myelodysplasia syndrome, somatic300448Graph: Alpha-thalassemia myelodysplasia syndrome, somaticMouseHumanRatWormXXXXXXXXX
Alpha-thalassemia/mental retardation syndrome301040Graph: Alpha-thalassemia/mental retardation syndromeMouseHumanRatWormXXXXXXXXX
Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity609889Graph: Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunityMouseHumanXXXXXXXXXXX
Alport syndrome301050Graph: Alport syndromeMouseHumanXWormXXXXXXXXX
Alport syndrome, autosomal recessive203780Graph: Alport syndrome, autosomal recessiveMouseHumanXXXXXXXXXXX
Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis300194Graph: Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosisXXXXXXXXXXXXX
Alstrom syndrome203800Graph: Alstrom syndromeMouseHumanXXXXXXXXXXX
Alternating hemiplegia of childhood104290Graph: Alternating hemiplegia of childhoodMouseXRatWormXXXZfinXXXXX
Alveolar soft-part sarcoma606243Graph: Alveolar soft-part sarcomaMouseXXXXXXXXXXXX
Alzheimer disease, type 3607822Graph: Alzheimer disease, type 3MouseHumanRatXXXXXXXXXX
Alzheimer disease, type 3, with spastic paraparesis and apraxia607822Graph: Alzheimer disease, type 3, with spastic paraparesis and apraxiaMouseHumanRatXXXXXXXXXX
Alzheimer disease, type 3, with spastic paraparesis and unusual plaques607822Graph: Alzheimer disease, type 3, with spastic paraparesis and unusual plaquesMouseHumanRatXXXXXXXXXX
Alzheimer disease-2104310Graph: Alzheimer disease-2MouseHumanRatXXXXXXXXXX
Alzheimer disease-4606889Graph: Alzheimer disease-4MouseHumanRatXXXXXXXXXX
Amelogenesis imperfecta 2, hypoplastic local104500Graph: Amelogenesis imperfecta 2, hypoplastic localXXXXXXXXXXXXX
Amelogenesis imperfecta, hypomaturation-hypoplastic type, with taurodontism104510Graph: Amelogenesis imperfecta, hypomaturation-hypoplastic type, with taurodontismXHumanXWormXXXZfinXXXXX
Amelogenesis imperfecta, hypoplastic, and openbite malocclusion608563Graph: Amelogenesis imperfecta, hypoplastic, and openbite malocclusionXXXXXXXXXXXXX
Amelogenesis imperfecta, hypoplastic/hypomaturation type301200Graph: Amelogenesis imperfecta, hypoplastic/hypomaturation typeMouseXRatXXXXXXXXXX
Amyloidosis, Finnish type105120Graph: Amyloidosis, Finnish typeMouseHumanRatXXXXXXXXXX
Amyloidosis, cerebroarterial, Iowa type605714Graph: Amyloidosis, cerebroarterial, Iowa typeMouseHumanRatXXXXXXXXXX
Amyloidosis, hereditary renal105200Graph: Amyloidosis, hereditary renalMouseHumanXXXXXZfinXXXXX
Amyloidosis, renal105200Graph: Amyloidosis, renalMouseHumanXXXXXZfinXXXXX
Amyotrophic lateral sclerosis 8608627Graph: Amyotrophic lateral sclerosis 8XHumanXXXXXXXXYeastXX
Amyotrophic lateral sclerosis, due to SOD1 deficiency105400Graph: Amyotrophic lateral sclerosis, due to SOD1 deficiencyMouseHumanRatXXXXXXXYeastXX
Amyotrophic lateral sclerosis, juvenile205100Graph: Amyotrophic lateral sclerosis, juvenileMouseHumanXXXXXXXXXXX
Anderson disease607689Graph: Anderson diseaseXXXXXXXXXXYeastXX
Androgen insensitivity300068Graph: Androgen insensitivityMouseHumanRatXXXXXXXXXX
Anemia, Diamond-Blackfan105650Graph: Anemia, Diamond-BlackfanXHumanXWormXXXXXXYeastXX
Anemia, congenital dyserythropoietic, type I224120Graph: Anemia, congenital dyserythropoietic, type IMouseXXXXXXXXXXXX
Anemia, hemolytic, Rh-null, regulator type268150Graph: Anemia, hemolytic, Rh-null, regulator typeXHumanXWormXDictyXXRiceXYeastXX
Anemia, hemolytic, due to UMPH1 deficiency266120Graph: Anemia, hemolytic, due to UMPH1 deficiencyXHumanXXXXXXXXXXX
Anemia, sideroblastic, with ataxia301310Graph: Anemia, sideroblastic, with ataxiaMouseHumanXXXXXXXXYeastXX
Angelman syndrome105830Graph: Angelman syndromeMouseHumanXXXXXXXXYeastXX
Angioedema, hereditary106100Graph: Angioedema, hereditaryXHumanXXXXXXXXXXX
Aniridia, type II106210Graph: Aniridia, type IIMouseHumanRatWormXXChickenXXXYeastXX
Anophthalmia 3206900Graph: Anophthalmia 3MouseXXXXXXXXXXXX
Anterior segment mesenchymal dysgenesis107250Graph: Anterior segment mesenchymal dysgenesisMouseHumanXXXXXXXXYeastXX
Anterior segment mesenchymal dysgenesis and cataract107250Graph: Anterior segment mesenchymal dysgenesis and cataractMouseHumanXXXXXXXXYeastXX
Antley-Bixler syndrome-like with disordered steroidogenesis201750Graph: Antley-Bixler syndrome-like with disordered steroidogenesisMouseHumanXXXXXXXXYeastXX
Anxiety-related personality traits607834Graph: Anxiety-related personality traitsXHumanRatXXXXXXXXXX
Aortic aneurysm, familial thoracic 3608967Graph: Aortic aneurysm, familial thoracic 3MouseHumanRatXXXXXXXXXX
Apert syndrome101200Graph: Apert syndromeMouseXXWormXXXXXXXXX
Aplastic anemia609135Graph: Aplastic anemiaMouseHumanRatXXXXXXXXXX
Argininemia207800Graph: ArgininemiaMouseHumanRatXXXXXXXYeastXX
Argininosuccinic aciduria207900Graph: Argininosuccinic aciduriaXHumanXXXXXXXXYeastXX
Aromatic L-amino acid decarboxylase deficiency608643Graph: Aromatic L-amino acid decarboxylase deficiencyXHumanRatXXXXXXXXXX
Arrhythmogenic right ventricular dysplasia 2600996Graph: Arrhythmogenic right ventricular dysplasia 2XHumanXWormXXXXXXXXX
Arrhythmogenic right ventricular dysplasia 8607450Graph: Arrhythmogenic right ventricular dysplasia 8XHumanXXXXXXXXXXX
Arrhythmogenic right ventricular dysplasia-5604400Graph: Arrhythmogenic right ventricular dysplasia-5XXRatWormXXXXXXYeastXX
Arterial calcification, generalized, of infancy208000Graph: Arterial calcification, generalized, of infancyMouseHumanXXXXXXXXXXX
Arthrogryposis multiplex congenita, distal, type 1108120Graph: Arthrogryposis multiplex congenita, distal, type 1XHumanRatWormXXXXXXYeastXX
Arthrogryposis multiplex congenita, distal, type 2B601680Graph: Arthrogryposis multiplex congenita, distal, type 2BXXXWormXXXXXXYeastXX
Arthropathy, progressive pseudorheumatoid, of childhood208230Graph: Arthropathy, progressive pseudorheumatoid, of childhoodXHumanXXFlyXXXXXXXX
Arthyrgryposis, distal, type 2B601680Graph: Arthyrgryposis, distal, type 2BXXXWormXXXXXXYeastXX
Ataxia with isolated vitamin E deficiency277460Graph: Ataxia with isolated vitamin E deficiencyMouseHumanRatXXXXXXXXXX
Ataxia, cerebellar, Cayman type601238Graph: Ataxia, cerebellar, Cayman typeXXXXXXXXXXXXX
Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia208920Graph: Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemiaMouseHumanXXXXXXXXYeastXX
Ataxia-ocular apraxia-2606002Graph: Ataxia-ocular apraxia-2XXXXXXXXXXXXX
Ataxia-telangiectasia208900Graph: Ataxia-telangiectasiaMouseHumanXXXXXXXXXXX
Ataxia-telangiectasia-like disorder604391Graph: Ataxia-telangiectasia-like disorderMouseHumanRatXXXXXXXYeastXX
Atelosteogenesis II256050Graph: Atelosteogenesis IIXHumanRatXXXXXXXXXX
Atelostogenesis, type I108720Graph: Atelostogenesis, type IMouseHumanXXXDictyXXXXXXX
Atopy147050Graph: AtopyMouseHumanXXXXXXXXXXX
Atransferrinemia209300Graph: AtransferrinemiaXHumanRatXXXXXXXXXX
Atrial fibrillation, familial607554Graph: Atrial fibrillation, familialMouseHumanRatXXXXXXXXXX
Atrial septal defect with atrioventricular conduction defects108900Graph: Atrial septal defect with atrioventricular conduction defectsMouseXRatWormXXXXXXXXX
Atrial septal defect-2607941Graph: Atrial septal defect-2MouseHumanRatWormXXXXXXXXX
Atrichia with papular lesions209500Graph: Atrichia with papular lesionsXXXXXXXXXXXXX
Atrioventricular septal defect600309Graph: Atrioventricular septal defectMouseHumanRatXXXXZfinXXXXX
Atrioventricular septal defect, partial, with heterotaxy syndrome606217Graph: Atrioventricular septal defect, partial, with heterotaxy syndromeXXXXXXXXXXXXX
Autoimmune lymphoproliferative syndrome, type IA601859Graph: Autoimmune lymphoproliferative syndrome, type IAMouseHumanRatXXXXXXXXXX
Autoimmune lymphoproliferative syndrome, type II603909Graph: Autoimmune lymphoproliferative syndrome, type IIXHumanXXXXXXXXXXX
Autoimmune lymphoproliferative syndrome, type IIB607271Graph: Autoimmune lymphoproliferative syndrome, type IIBMouseHumanRatXXXXXXXXXX
Autoimmune polyglandular disease, type I240300Graph: Autoimmune polyglandular disease, type IXHumanXXXXXXXXXXX
Azoospermia415000Graph: AzoospermiaMouseHumanRatXXXXXXXXXX

B
OMIM disorder(s)OMIM_idComparisonGraphMouseHumanRatWormFlyDictyChickenZfinRiceTairYeastPombePfalc
BCG and salmonella infection, disseminated209950Graph: BCG and salmonella infection, disseminatedMouseHumanRatXXXXXXXXXX
BCG infection, generalized familial209950Graph: BCG infection, generalized familialMouseHumanRatXXXXXXXXXX
Baller-Gerold syndrome218600Graph: Baller-Gerold syndromeXHumanXXXXXXXXXXX
Bannayan-Riley-Ruvalcaba syndrome153480Graph: Bannayan-Riley-Ruvalcaba syndromeMouseHumanRatWormXDictyXXXXXXX
Bannayan-Zonana syndrome153480Graph: Bannayan-Zonana syndromeMouseHumanRatWormXDictyXXXXXXX
Bardet-Biedl syndrome 1209900Graph: Bardet-Biedl syndrome 1MouseHumanRatXXXXXXXXXX
Bardet-Biedl syndrome 1, modifier of209900Graph: Bardet-Biedl syndrome 1, modifier ofMouseHumanRatXXXXXXXXXX
Bardet-Biedl syndrome 2209900Graph: Bardet-Biedl syndrome 2MouseHumanRatXXXXXXXXXX
Bardet-Biedl syndrome 3209900Graph: Bardet-Biedl syndrome 3MouseHumanRatXXXXXXXXXX
Bardet-Biedl syndrome 4209900Graph: Bardet-Biedl syndrome 4MouseHumanRatXXXXXXXXXX
Bardet-Biedl syndrome 5209900Graph: Bardet-Biedl syndrome 5MouseHumanRatXXXXXXXXXX
Bardet-Biedl syndrome 6209900Graph: Bardet-Biedl syndrome 6MouseHumanRatXXXXXXXXXX
Bardet-Biedl syndrome 7209900Graph: Bardet-Biedl syndrome 7MouseHumanRatXXXXXXXXXX
Bardet-Biedl syndrome 8209900Graph: Bardet-Biedl syndrome 8MouseHumanRatXXXXXXXXXX
Bare lymphocyte syndrome, type I604571Graph: Bare lymphocyte syndrome, type IMouseHumanRatXXXXXXXXXX
Bare lymphocyte syndrome, type I, due to TAP2 deficiency604571Graph: Bare lymphocyte syndrome, type I, due to TAP2 deficiencyMouseHumanRatXXXXXXXXXX
Bare lymphocyte syndrome, type II, complementation group A209920Graph: Bare lymphocyte syndrome, type II, complementation group AMouseHumanRatXXXXXXXXXX
Bare lymphocyte syndrome, type II, complementation group C209920Graph: Bare lymphocyte syndrome, type II, complementation group CMouseHumanRatXXXXXXXXXX
Bare lymphocyte syndrome, type II, complementation group D209920Graph: Bare lymphocyte syndrome, type II, complementation group DMouseHumanRatXXXXXXXXXX
Bare lymphocyte syndrome, type II, complementation group E209920Graph: Bare lymphocyte syndrome, type II, complementation group EMouseHumanRatXXXXXXXXXX
Bart-Pumphrey syndrome149200Graph: Bart-Pumphrey syndromeMouseHumanRatXXXXXXXXXX
Barth syndrome302060Graph: Barth syndromeXHumanXXXXXXXXYeastXX
Bartter syndrome, type 1601678Graph: Bartter syndrome, type 1XHumanXXXXXXXXXXX
Bartter syndrome, type 2241200Graph: Bartter syndrome, type 2XHumanXXXXXXXXXXX
Bartter syndrome, type 3607364Graph: Bartter syndrome, type 3MouseHumanRatXXXXXXXXXX
Bartter syndrome, type 4602522Graph: Bartter syndrome, type 4MouseHumanRatXXXXXXXXXX
Bartter syndrome, type 4, digenic602522Graph: Bartter syndrome, type 4, digenicMouseHumanRatXXXXXXXXXX
Basal cell carcinoma, somatic605462Graph: Basal cell carcinoma, somaticMouseHumanXWormXXXXXXXXX
Basal cell nevus syndrome109400Graph: Basal cell nevus syndromeMouseHumanXWormXXXXXXXXX
Basal ganglia disease, adult-onset606159Graph: Basal ganglia disease, adult-onsetXHumanXXXXXXXXXXX
Beare-Stevenson cutis gyrata syndrome123790Graph: Beare-Stevenson cutis gyrata syndromeMouseXXWormXXXXXXXXX
Becker muscular dystrophy300376Graph: Becker muscular dystrophyMouseHumanXXXXXZfinXXXXX
Becker muscular dystrophy modifier310200Graph: Becker muscular dystrophy modifierMouseHumanXWormXXXZfinXXXXX
Beckwith-Wiedemann syndrome130650Graph: Beckwith-Wiedemann syndromeMouseHumanXWormXXXZfinXXXXX
Bernard-Soulier syndrome, type A231200Graph: Bernard-Soulier syndrome, type AMouseHumanXXXXXXXXXXX
Bernard-Soulier syndrome, type C231200Graph: Bernard-Soulier syndrome, type CMouseHumanXXXXXXXXXXX
Bethlem myopathy158810Graph: Bethlem myopathyMouseHumanXXXXXXXXXXX
Birt-Hogg-Dube syndrome135150Graph: Birt-Hogg-Dube syndromeXXXXXXXXXXXXX
Bladder cancer109800Graph: Bladder cancerMouseHumanXWormXDictyXXXXXXX
Blau syndrome186580Graph: Blau syndromeMouseHumanXXXXXXXXXXX
Bleeding disorder due to P2RY12 defect609821Graph: Bleeding disorder due to P2RY12 defectMouseXRatXXXXXXXXXX
Blepharophimosis, epicanthus inversus, and ptosis, type 1110100Graph: Blepharophimosis, epicanthus inversus, and ptosis, type 1MouseXXXXXXXXXXXX
Blepharophimosis, epicanthus inversus, and ptosis, type 2110100Graph: Blepharophimosis, epicanthus inversus, and ptosis, type 2MouseXXXXXXXXXXXX
Bloom syndrome210900Graph: Bloom syndromeMouseHumanXXXXXXXXXXX
Blue-cone monochromacy303700Graph: Blue-cone monochromacyMouseHumanXXXXXXXXXXX
Borjeson-Forssman-Lehmann syndrome301900Graph: Borjeson-Forssman-Lehmann syndromeXXXXXXXXXXXXX
Bothnia retinal dystrophy607475Graph: Bothnia retinal dystrophyMouseHumanXXXXXXXXXXX
Brachydactyly, type A1112500Graph: Brachydactyly, type A1MouseXXWormXXXXXXXXX
Brachydactyly, type A2112600Graph: Brachydactyly, type A2MouseHumanXWormXXXXXXXXX
Brachydactyly, type B1113000Graph: Brachydactyly, type B1MouseHumanXWormXXXXXXXXX
Brachydactyly, type C113100Graph: Brachydactyly, type CMouseHumanXXXXXXXXXXX
Brachydactyly, type D113200Graph: Brachydactyly, type DMouseHumanXXXXXXXXXXX
Brachydactyly, type E113300Graph: Brachydactyly, type EMouseHumanXXXXXXXXXXX
Bradyopsia608415Graph: BradyopsiaMouseHumanRatXXXXXXXXXX
Branchiootorenal syndrome113650Graph: Branchiootorenal syndromeMouseHumanXXXXXXXXXXX
Branchiootorenal syndrome with cataract113650Graph: Branchiootorenal syndrome with cataractMouseHumanXXXXXXXXXXX
Breast cancer114480Graph: Breast cancerMouseHumanRatWormXDictyXXXXXXX
Breast cancer, early-onset114480Graph: Breast cancer, early-onsetMouseHumanRatWormXDictyXXXXXXX
Breast cancer, somatic114480Graph: Breast cancer, somaticMouseHumanRatWormXDictyXXXXXXX
Brody myopathy601003Graph: Brody myopathyMouseHumanRatWormXXXZfinXXXXX
Brugada syndrome601144Graph: Brugada syndromeXHumanRatXXXXXXXXXX
Burkitt lymphoma113970Graph: Burkitt lymphomaMouseHumanRatXXXXXXXXXX
Butterfly dystrophy, retinal169150Graph: Butterfly dystrophy, retinalXHumanXXXXXXXXXXX

C
OMIM disorder(s)OMIM_idComparisonGraphMouseHumanRatWormFlyDictyChickenZfinRiceTairYeastPombePfalc
CHILD syndrome308050Graph: CHILD syndromeMouseHumanXXXXXXXXYeastXX
CINCA syndrome607115Graph: CINCA syndromeXHumanXXXDictyXXXXXXX
CPT II deficiency, lethal neonatal608836Graph: CPT II deficiency, lethal neonatalMouseXRatXXXXXXXYeastXX
CPT deficiency, hepatic, type IA255120Graph: CPT deficiency, hepatic, type IAMouseHumanRatXXXXXXXXXX
CPT deficiency, hepatic, type II600649Graph: CPT deficiency, hepatic, type IIMouseXRatXXXXXXXYeastXX
CRASH syndrome303350Graph: CRASH syndromeMouseHumanXXXXXZfinXXXXX
Cafe-au-lait spots with glioma or leukemia114030Graph: Cafe-au-lait spots with glioma or leukemiaMouseHumanXXXXXXXXYeastXX
Caffey disease114000Graph: Caffey diseaseXHumanXXXXXXXXXXX
Calcinosis, tumoral211900Graph: Calcinosis, tumoralMouseXXXXXXXXXXXX
Campomelic dysplasia114290Graph: Campomelic dysplasiaMouseHumanXXXXXZfinXXXXX
Campomelic dysplasia with autosomal sex reversal114290Graph: Campomelic dysplasia with autosomal sex reversalMouseHumanXXXXXZfinXXXXX
Camptodactyly-arthropathy-coxa vara-pericarditis syndrome208250Graph: Camptodactyly-arthropathy-coxa vara-pericarditis syndromeXHumanXXXXXXXXXXX
Camurati-Engelmann disease131300Graph: Camurati-Engelmann diseaseMouseHumanRatXXXXXXXXXX
Canavan disease271900Graph: Canavan diseaseMouseHumanRatXXXXXXXXXX
Capillary malformation-arteriovenous malformation608354Graph: Capillary malformation-arteriovenous malformationMouseHumanXXXXXXXXXXX
Carbamoylphosphate synthetase I deficiency237300Graph: Carbamoylphosphate synthetase I deficiencyXHumanXXXXXXXXXXX
Carbohydrate-deficient glycoprotein syndrome, type I212065Graph: Carbohydrate-deficient glycoprotein syndrome, type IXHumanXXXXXXXXYeastPombeX
Carbohydrate-deficient glycoprotein syndrome, type II212066Graph: Carbohydrate-deficient glycoprotein syndrome, type IIMouseHumanXXXXXXXXXXX
Carbohydrate-deficient glycoprotein syndrome, type Ib602579Graph: Carbohydrate-deficient glycoprotein syndrome, type IbXHumanXXXXXXXXYeastXX
Carboxypeptidase N deficiency212070Graph: Carboxypeptidase N deficiencyMouseHumanRatXXXXXXXXXX
Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency604377Graph: Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiencyXHumanXXXXXXXXYeastXX
Cardiofaciocutaneous syndrome115150Graph: Cardiofaciocutaneous syndromeMouseHumanXWormXXXXXXXXX
Cardiomopathy, Familial hypertrophic, 8608751Graph: Cardiomopathy, Familial hypertrophic, 8XHumanXXXXXXXXXXX
Cardiomyopathy, X-linked dilated300069Graph: Cardiomyopathy, X-linked dilatedXHumanXXXXXXXXYeastXX
Cardiomyopathy, dilated115200Graph: Cardiomyopathy, dilatedMouseHumanRatWormXXXXXXXXX
Cardiomyopathy, dilated, 1A115200Graph: Cardiomyopathy, dilated, 1AMouseHumanRatWormXXXXXXXXX
Cardiomyopathy, dilated, 1D601494Graph: Cardiomyopathy, dilated, 1DMouseHumanRatWormXXXZfinXXYeastXX
Cardiomyopathy, dilated, 1E601154Graph: Cardiomyopathy, dilated, 1EXHumanRatXXXXXXXXXX
Cardiomyopathy, dilated, 1G604145Graph: Cardiomyopathy, dilated, 1GMouseHumanRatWormXXXXXXXXPfalc
Cardiomyopathy, dilated, 1I604765Graph: Cardiomyopathy, dilated, 1IMouseHumanXXXXXXXXXXX
Cardiomyopathy, dilated, 1J605362Graph: Cardiomyopathy, dilated, 1JXHumanXXXXXXXXXXX
Cardiomyopathy, dilated, 1L606685Graph: Cardiomyopathy, dilated, 1LMouseHumanXXXXXXXXXXX
Cardiomyopathy, dilated, 1M607482Graph: Cardiomyopathy, dilated, 1MMouseHumanXXXXXXXXXXX
Cardiomyopathy, dilated, 1N607487Graph: Cardiomyopathy, dilated, 1NXHumanXXXXXXXXXXX
Cardiomyopathy, dilated, 1O608569Graph: Cardiomyopathy, dilated, 1OXHumanRatXXXXXXXXXX
Cardiomyopathy, dilated, X-linked302045Graph: Cardiomyopathy, dilated, X-linkedMouseHumanXXXXXZfinXXXXX
Cardiomyopathy, familial hypertrophic192600Graph: Cardiomyopathy, familial hypertrophicMouseHumanRatWormXDictyXXRiceXYeastPombeX
Cardiomyopathy, familial hypertrophic, 1192600Graph: Cardiomyopathy, familial hypertrophic, 1MouseHumanRatWormXDictyXXRiceXYeastPombeX
Cardiomyopathy, familial hypertrophic, 10608758Graph: Cardiomyopathy, familial hypertrophic, 10XHumanXWormXXXXXXXXX
Cardiomyopathy, familial hypertrophic, 2115195Graph: Cardiomyopathy, familial hypertrophic, 2MouseHumanRatWormXXXZfinXXYeastXX
Cardiomyopathy, familial hypertrophic, 3115196Graph: Cardiomyopathy, familial hypertrophic, 3XHumanRatWormXXXXXXYeastXX
Cardiomyopathy, familial hypertrophic, 4115197Graph: Cardiomyopathy, familial hypertrophic, 4MouseHumanXXXXXXXXXXX
Cardiomyopathy, familial restrictive115210Graph: Cardiomyopathy, familial restrictiveMouseHumanRatWormXXXXXXXXX
Cardiomyopathy, hypertrophic, mid-left ventricular chamber type608758Graph: Cardiomyopathy, hypertrophic, mid-left ventricular chamber typeXHumanXWormXXXXXXXXX
Cardiomyopathy, hypertrophic, midventricular, digenic192600Graph: Cardiomyopathy, hypertrophic, midventricular, digenicMouseHumanRatWormXDictyXXRiceXYeastPombeX
Cardiomyopathy, hypertrophic, with WPW600858Graph: Cardiomyopathy, hypertrophic, with WPWMouseXXXXXXXXXYeastXX
Carney complex variant608837Graph: Carney complex variantXHumanXWormXDictyXXXXYeastPombeX
Carney complex, type 1160980Graph: Carney complex, type 1MouseHumanRatWormXDictyXXXXXXX
Carnitine deficiency, systemic primary212140Graph: Carnitine deficiency, systemic primaryXHumanRatXXXXXXXXXX
Cataract, Coppock-like604307Graph: Cataract, Coppock-likeMouseXXXXXXXXXXXX
Cataract, Marner type116800Graph: Cataract, Marner typeMouseHumanXWormXXXXXTairXXX
Cataract, cerulean, type 2601547Graph: Cataract, cerulean, type 2MouseHumanXXXXXXXXXXX
Cataract, congenital604219Graph: Cataract, congenitalMouseHumanXXXXXXXXYeastXX
Cataract, congenital zonular, with sutural opacities600881Graph: Cataract, congenital zonular, with sutural opacitiesMouseHumanXXXXXXXXXXX
Cataract, congenital, cerulean type, 3608983Graph: Cataract, congenital, cerulean type, 3MouseHumanXXXXXXXXXXX
Cataract, crystalline aculeiform115700Graph: Cataract, crystalline aculeiformMouseHumanXXXXXXXXXXX
Cataract, juvenile-onset604219Graph: Cataract, juvenile-onsetMouseHumanXXXXXXXXYeastXX
Cataract, lamellar116800Graph: Cataract, lamellarMouseHumanXWormXXXXXTairXXX
Cataract, polymorphic and lamellar604219Graph: Cataract, polymorphic and lamellarMouseHumanXXXXXXXXYeastXX
Cataract, sutural, with punctate and cerulean opacities607133Graph: Cataract, sutural, with punctate and cerulean opacitiesMouseHumanXXXXXXXXXXX
Cataract, zonular pulverulent-1116200Graph: Cataract, zonular pulverulent-1MouseHumanXXXXXXXXXXX
Cataract, zonular pulverulent-3601885Graph: Cataract, zonular pulverulent-3MouseHumanRatXXXXXXXXXX
Cavernous malformations of CNS and retina116860Graph: Cavernous malformations of CNS and retinaXHumanXXXXXXXXXXX
Central core disease117000Graph: Central core diseaseMouseHumanXWormXXXXXXXXX
Central hypoventilation syndrome209880Graph: Central hypoventilation syndromeMouseHumanRatXXXXZfinXXXXX
Central hypoventilation syndrome, congenital209880Graph: Central hypoventilation syndrome, congenitalMouseHumanRatXXXXZfinXXXXX
Cerebellar ataxia604290Graph: Cerebellar ataxiaXHumanRatXXXXXXXXXX
Cerebral amyloid angiopathy105150Graph: Cerebral amyloid angiopathyXHumanXXXXXXXXXXX
Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy125310Graph: Cerebral arteriopathy with subcortical infarcts and leukoencephalopathyMouseXRatXXXXXXXXXX
Cerebral cavernous malformations-1116860Graph: Cerebral cavernous malformations-1XHumanXXXXXXXXXXX
Cerebral cavernous malformations-2603284Graph: Cerebral cavernous malformations-2XXXXXXXXXXXXX
Cerebrooculofacioskeletal syndrome214150Graph: Cerebrooculofacioskeletal syndromeMouseHumanXXXXXXXXYeastXX
Cerebrotendinous xanthomatosis213700Graph: Cerebrotendinous xanthomatosisMouseHumanRatXXXXXXXXXX
Ceroid lipofuscinosis, neuronal 8600143Graph: Ceroid lipofuscinosis, neuronal 8XHumanXXXXXXXXXXX
Ceroid lipofuscinosis, neuronal-1, infantile256730Graph: Ceroid lipofuscinosis, neuronal-1, infantileMouseHumanRatXXXXXXXXXX
Ceroid-lipofuscinosis, neuronal 2, classic late infantile204500Graph: Ceroid-lipofuscinosis, neuronal 2, classic late infantileXXXXXXXXXXXXX
Ceroid-lipofuscinosis, neuronal-3, juvenile204200Graph: Ceroid-lipofuscinosis, neuronal-3, juvenileXHumanXWormXXXXXXYeastXX
Ceroid-lipofuscinosis, neuronal-5, variant late infantile256731Graph: Ceroid-lipofuscinosis, neuronal-5, variant late infantileMouseHumanXXXXXXXXXXX
Ceroid-lipofuscinosis, neuronal-6, variant late infantile601780Graph: Ceroid-lipofuscinosis, neuronal-6, variant late infantileXXXXXXXXXXXXX
Cervical cancer, somatic603956Graph: Cervical cancer, somaticMouseHumanXWormXXXXXXXXX
Chanarin-Dorfman syndrome275630Graph: Chanarin-Dorfman syndromeMouseXXXXXXXXXYeastXX
Char syndrome169100Graph: Char syndromeMouseHumanXXXXXXXXXXX
Charcot-Marie-Tooth disease, axonal, type 2F606595Graph: Charcot-Marie-Tooth disease, axonal, type 2FMouseHumanXXXXXXXXXXX
Charcot-Marie-Tooth disease, dominant intermediate 3607791Graph: Charcot-Marie-Tooth disease, dominant intermediate 3MouseHumanXXXXXXXXXXX
Charcot-Marie-Tooth disease, mixed axonal and demyelinating type214400Graph: Charcot-Marie-Tooth disease, mixed axonal and demyelinating typeXXXXXXXXXXXXX
Charcot-Marie-Tooth disease, type 1A118220Graph: Charcot-Marie-Tooth disease, type 1AXHumanRatXXXXXXXXXX
Charcot-Marie-Tooth disease, type 1B118200Graph: Charcot-Marie-Tooth disease, type 1BMouseHumanXXXXXXXXXXX
Charcot-Marie-Tooth disease, type 1C601098Graph: Charcot-Marie-Tooth disease, type 1CMouseHumanXXXXXXXXXXX
Charcot-Marie-Tooth disease, type 1D607678Graph: Charcot-Marie-Tooth disease, type 1DMouseHumanRatXXXXXXXYeastXX
Charcot-Marie-Tooth disease, type 1E118300Graph: Charcot-Marie-Tooth disease, type 1EXHumanRatXXXXXXXXXX
Charcot-Marie-Tooth disease, type 1F607734Graph: Charcot-Marie-Tooth disease, type 1FMouseHumanRatXXXXXXXXXX
Charcot-Marie-Tooth disease, type 2A1118210Graph: Charcot-Marie-Tooth disease, type 2A1MouseHumanXWormXXXXXXXXX
Charcot-Marie-Tooth disease, type 2A2609260Graph: Charcot-Marie-Tooth disease, type 2A2MouseHumanXWormXXXXXXXXX
Charcot-Marie-Tooth disease, type 2B600882Graph: Charcot-Marie-Tooth disease, type 2BMouseHumanRatWormXXXXXXYeastXX
Charcot-Marie-Tooth disease, type 2D601472Graph: Charcot-Marie-Tooth disease, type 2DMouseHumanXWormXXXXXXYeastXX
Charcot-Marie-Tooth disease, type 2E607684Graph: Charcot-Marie-Tooth disease, type 2EMouseHumanRatXXXXXXXXXX
Charcot-Marie-Tooth disease, type 2G607706Graph: Charcot-Marie-Tooth disease, type 2GXXXXXXXXXXXXX
Charcot-Marie-Tooth disease, type 2I607677Graph: Charcot-Marie-Tooth disease, type 2IMouseHumanXXXXXXXXXXX
Charcot-Marie-Tooth disease, type 2J607736Graph: Charcot-Marie-Tooth disease, type 2JMouseHumanXXXXXXXXXXX
Charcot-Marie-Tooth disease, type 2K607831Graph: Charcot-Marie-Tooth disease, type 2KXXXXXXXXXXXXX
Charcot-Marie-Tooth disease, type 4A214400Graph: Charcot-Marie-Tooth disease, type 4AXXXXXXXXXXXXX
Charcot-Marie-Tooth disease, type 4B1601382Graph: Charcot-Marie-Tooth disease, type 4B1MouseHumanXXXXXXXXYeastXX
Charcot-Marie-Tooth disease, type 4B2604563Graph: Charcot-Marie-Tooth disease, type 4B2XXXXXXXXXXXXX
Charcot-Marie-Tooth disease, type 4D601455Graph: Charcot-Marie-Tooth disease, type 4DXHumanXXXXXXXXXXX
Charcot-Marie-Tooth neuropathy, X-linked dominant, 1302800Graph: Charcot-Marie-Tooth neuropathy, X-linked dominant, 1XHumanRatXXXXXXXXXX
Chediak-Higashi syndrome214500Graph: Chediak-Higashi syndromeXHumanXXXXXXXXXXX
Cherubism118400Graph: CherubismXHumanXXXXXXXXXXX
Chloride diarrhea, congenital, Finnish type214700Graph: Chloride diarrhea, congenital, Finnish typeMouseHumanRatXXXXXXXXXX
Cholestasis, benign recurrent intrahepatic243300Graph: Cholestasis, benign recurrent intrahepaticMouseHumanXXXXXXXXXXX
Cholestasis, familial intrahepatic, of pregnancy147480Graph: Cholestasis, familial intrahepatic, of pregnancyMouseHumanXWormXDictyXXXXYeastXPfalc
Cholestasis, progressive familial intrahepatic 1211600Graph: Cholestasis, progressive familial intrahepatic 1MouseHumanXXXXXXXXXXX
Cholestasis, progressive familial intrahepatic 2601847Graph: Cholestasis, progressive familial intrahepatic 2MouseHumanRatWormXDictyXXXXYeastXPfalc
Cholestasis, progressive familial intrahepatic 3602347Graph: Cholestasis, progressive familial intrahepatic 3MouseHumanXWormXDictyXXXXYeastXPfalc
Cholestasis, progressive familial intrahepatic 4607765Graph: Cholestasis, progressive familial intrahepatic 4XHumanRatXXXXXXXXXX
Chondrocalcinosis 2118600Graph: Chondrocalcinosis 2MouseHumanXXXXXXXXXXX
Chondrodysplasia punctata, X-linked dominant302960Graph: Chondrodysplasia punctata, X-linked dominantMouseHumanRatXXXXXXXXXX
Chondrodysplasia punctata, X-linked recessive302950Graph: Chondrodysplasia punctata, X-linked recessiveXHumanXXXXXXXXXXX
Chondrodysplasia punctata, rhizomelic, type 2222765Graph: Chondrodysplasia punctata, rhizomelic, type 2MouseHumanRatXXXXXXXXXX
Chondrodysplasia, Grebe type200700Graph: Chondrodysplasia, Grebe typeMouseHumanXXXXXXXXXXX
Chondrosarcoma215300Graph: ChondrosarcomaMouseHumanXXXXXXXXXXX
Chorea, hereditary benign118700Graph: Chorea, hereditary benignMouseXRatWormXXXXXXXXX
Choreoacanthocytosis200150Graph: ChoreoacanthocytosisXXXXXXXXXXYeastXX
Choroideremia303100Graph: ChoroideremiaMouseHumanRatXXXXXXXXXX
Chromosome 22q13.3 deletion syndrome606232Graph: Chromosome 22q13.3 deletion syndromeXXXXXXXXXXXXX
Chronic granulomatous disease due to deficiency of NCF-1233700Graph: Chronic granulomatous disease due to deficiency of NCF-1MouseHumanXXXXXXXXXXX
Chronic granulomatous disease, X-linked306400Graph: Chronic granulomatous disease, X-linkedXHumanRatXXDictyXXXXYeastXX
Chronic granulomatous disease, autosomal, due to deficiency of CYBA233690Graph: Chronic granulomatous disease, autosomal, due to deficiency of CYBAXHumanRatXXXXXXXXXX
Chudley-Lowry syndrome309490Graph: Chudley-Lowry syndromeMouseHumanRatWormXXXXXXXXX
Chylomicron retention disease246700Graph: Chylomicron retention diseaseXXXXXXXXXXYeastXX
Chylomicron retention disease with Marinesco-Sjogren syndrome607692Graph: Chylomicron retention disease with Marinesco-Sjogren syndromeXXXXXXXXXXYeastXX
Ciliary dyskinesia, primary, 1242650Graph: Ciliary dyskinesia, primary, 1XHumanXXXXXXXXXXX
Cirrhosis, North American Indian childhood type604901Graph: Cirrhosis, North American Indian childhood typeXXXXXXXXXXYeastXX
Citrullinemia215700Graph: CitrullinemiaMouseHumanRatXXXXXXXYeastXX
Citrullinemia, adult-onset type II603471Graph: Citrullinemia, adult-onset type IIMouseHumanXXXXXXXXYeastXX
Citrullinemia, type II, neonatal-onset605814Graph: Citrullinemia, type II, neonatal-onsetMouseHumanXXXXXXXXYeastXX
Cleft lip/palate ectodermal dysplasia syndrome225000Graph: Cleft lip/palate ectodermal dysplasia syndromeMouseHumanXXXXXXXXXXX
Cleft lip/palate, nonsyndromic608874Graph: Cleft lip/palate, nonsyndromicMouseHumanXWormXXXXXXXXX
Cleft palate with ankyloglossia303400Graph: Cleft palate with ankyloglossiaXHumanXXXXXXXXXXX
Cleidocranial dysplasia119600Graph: Cleidocranial dysplasiaMouseHumanXXXXXXXXXXX
Coenzyme Q10 deficiency607426Graph: Coenzyme Q10 deficiencyMouseHumanXXXXXXXXYeastXX
Coffin-Lowry syndrome303600Graph: Coffin-Lowry syndromeMouseHumanXXXXXXXXXXX
Cohen syndrome216550Graph: Cohen syndromeXXXXXXXXXXXXX
Cold-induced autoinflammatory syndrome, familial120100Graph: Cold-induced autoinflammatory syndrome, familialXHumanXXXDictyXXXXXXX
Cold-induced sweating syndrome272430Graph: Cold-induced sweating syndromeXHumanXXXXXXXXXXX
Coloboma, ocular120200Graph: Coloboma, ocularMouseHumanRatWormXXChickenXXXYeastXX
Colon cancer, somatic114500Graph: Colon cancer, somaticMouseHumanRatWormXDictyXXXXYeastPombeX
Colorectal adenomatous polyposis, autosomal recessive, with pilomatricomas132600Graph: Colorectal adenomatous polyposis, autosomal recessive, with pilomatricomasMouseHumanRatWormXXXZfinXXXXX
Colorectal cancer114500Graph: Colorectal cancerMouseHumanRatWormXDictyXXXXYeastPombeX
Colorectal cancer, hereditary nonpolyposis, type 2609310Graph: Colorectal cancer, hereditary nonpolyposis, type 2MouseHumanXXXXXXXXYeastXX
Colorectal cancer, somatic114500Graph: Colorectal cancer, somaticMouseHumanRatWormXDictyXXXXYeastPombeX
Combined factor V and VIII deficiency227300Graph: Combined factor V and VIII deficiencyMouseHumanXXXXXXXXXXX
Combined immunodeficiency, X-linked, moderate312863Graph: Combined immunodeficiency, X-linked, moderateMouseHumanRatXXXXXXXXXX
Complex V, mitochondrial respiratory chain, deficiency of604273Graph: Complex V, mitochondrial respiratory chain, deficiency ofXXXXXXXXXXYeastXX
Cone dystrophy-1304020Graph: Cone dystrophy-1MouseHumanXXXXXXXXXXX
Cone dystrophy-3602093Graph: Cone dystrophy-3MouseHumanXXXXXXXXXXX
Cone-rod dystrophy300029Graph: Cone-rod dystrophyMouseHumanXXXXXXXXXXX
Cone-rod dystrophy 3604116Graph: Cone-rod dystrophy 3MouseHumanXXXXXXXXXXX
Cone-rod dystrophy 9608194Graph: Cone-rod dystrophy 9MouseXXXXXXXXXXXX
Cone-rod retinal dystrophy-2120970Graph: Cone-rod retinal dystrophy-2MouseHumanXXXXXXXXXXX
Congenital bilateral absence of vas deferens277180Graph: Congenital bilateral absence of vas deferensXHumanRatXXXXXXXXXX
Congenital disorder of glycosylation, type IIc266265Graph: Congenital disorder of glycosylation, type IIcXXXXXXXXXXXXX
Congenital disorder of glycosylation, type IId607091Graph: Congenital disorder of glycosylation, type IIdMouseXXXXXXXXXXXX
Congenital disorder of glycosylation, type IIe608779Graph: Congenital disorder of glycosylation, type IIeXHumanXXXXXXXXXXX
Congenital disorder of glycosylation, type Ic603147Graph: Congenital disorder of glycosylation, type IcXHumanXXXXXXXXYeastXX
Congenital disorder of glycosylation, type Id601110Graph: Congenital disorder of glycosylation, type IdXXXXXXXXXXXXX
Congenital disorder of glycosylation, type Ie608799Graph: Congenital disorder of glycosylation, type IeMouseHumanXXXXXXXXYeastXX
Congenital disorder of glycosylation, type Ig607143Graph: Congenital disorder of glycosylation, type IgXXXXXXXXXXXXX
Congenital disorder of glycosylation, type Ih608104Graph: Congenital disorder of glycosylation, type IhXXXXXXXXXXYeastXX
Congenital disorder of glycosylation, type Ii607906Graph: Congenital disorder of glycosylation, type IiXXXXXXXXXXYeastXX
Congenital disorder of glycosylation, type Ij608093Graph: Congenital disorder of glycosylation, type IjMouseXXXXXXXXXYeastXX
Congenital disorder of glycosylation, type Ik608540Graph: Congenital disorder of glycosylation, type IkXXXXXXXXXXYeastXX
Congenital disorder of glycosylation, type Il608776Graph: Congenital disorder of glycosylation, type IlXXXXXXXXXXYeastXX
Conjunctivitis, ligneous217090Graph: Conjunctivitis, ligneousMouseHumanXXXXXXXXXXX
Conotruncal anomaly face syndrome217095Graph: Conotruncal anomaly face syndromeXHumanXWormXXXXXXXXX
Convulsions, familial febrile, 4604352Graph: Convulsions, familial febrile, 4MouseHumanXXXXXXXXXXX
Cornea plana congenita, recessive217300Graph: Cornea plana congenita, recessiveXXXXXXXXXXXXX
Corneal dystrophy, Avellino type607541Graph: Corneal dystrophy, Avellino typeMouseHumanXXXXXXXXXXX
Corneal dystrophy, Groenouw type I121900Graph: Corneal dystrophy, Groenouw type IMouseHumanXXXXXXXXXXX
Corneal dystrophy, Reis-Bucklers type608470Graph: Corneal dystrophy, Reis-Bucklers typeMouseHumanXXXXXXXXXXX
Corneal dystrophy, Thiel-Behnke type602082Graph: Corneal dystrophy, Thiel-Behnke typeMouseHumanXXXXXXXXXXX
Corneal dystrophy, gelatinous drop-like204870Graph: Corneal dystrophy, gelatinous drop-likeXHumanXXXXXXXXXXX
Corneal dystrophy, hereditary polymorphous posterior122000Graph: Corneal dystrophy, hereditary polymorphous posteriorMouseHumanXWormXXXXXXYeastXX
Corneal dystrophy, lattice type I122200Graph: Corneal dystrophy, lattice type IMouseHumanXXXXXXXXXXX
Corneal dystrophy, lattice type IIIA608471Graph: Corneal dystrophy, lattice type IIIAMouseHumanXXXXXXXXXXX
Cornelia de Lange syndrome122470Graph: Cornelia de Lange syndromeXXXWormXXXXXXYeastXX
Coronary artery disease, autosomal dominant, 1608320Graph: Coronary artery disease, autosomal dominant, 1MouseHumanXXXXXXXXXXX
Corpus callosum, agenesis of, with mental retardation, ocular coloboma and micrognathia300472Graph: Corpus callosum, agenesis of, with mental retardation, ocular coloboma and micrognathiaXHumanXXXXXXXXYeastXX
Cortisone reductase deficiency604931Graph: Cortisone reductase deficiencyMouseHumanRatXXXXXXXXXX
Costello syndrome218040Graph: Costello syndromeMouseHumanXWormXDictyXXXXXXX
Coumarin resistance122700Graph: Coumarin resistanceMouseHumanRatXXXXXXXXXX
Cowden disease158350Graph: Cowden diseaseMouseHumanRatWormXDictyXXXXXXX
Cowden-like syndrome158350Graph: Cowden-like syndromeMouseHumanRatWormXDictyXXXXXXX
Craniofacial-deafness-hand syndrome122880Graph: Craniofacial-deafness-hand syndromeMouseHumanXXXXXXXXYeastXX
Craniofrontonasal dysplasia304110Graph: Craniofrontonasal dysplasiaMouseHumanRatXXXXXXXXXX
Craniometaphyseal dysplasia123000Graph: Craniometaphyseal dysplasiaMouseHumanXXXXXXXXXXX
Craniosynostosis, type 2604757Graph: Craniosynostosis, type 2MouseHumanXWormXXXXXXXXX
Creatine deficiency syndrome, X-linked300352Graph: Creatine deficiency syndrome, X-linkedXHumanRatXXXXXXXXXX
Creatine phosphokinase, elevated serum123320Graph: Creatine phosphokinase, elevated serumMouseHumanRatWormXXXXXXXXX
Creutzfeldt-Jakob disease123400Graph: Creutzfeldt-Jakob diseaseMouseHumanRatXXXXXXXXXX
Crigler-Najjar syndrome, type I218800Graph: Crigler-Najjar syndrome, type IXXRatXXDictyXXXXXXX
Crigler-Najjar syndrome, type II606785Graph: Crigler-Najjar syndrome, type IIXXRatXXDictyXXXXXXX
Crouzon syndrome123500Graph: Crouzon syndromeMouseXXWormXXXXXXXXX
Cryptorchidism, idiopathic219050Graph: Cryptorchidism, idiopathicMouseHumanXXXXXXXXXXX
Currarino syndrome176450Graph: Currarino syndromeXHumanXXXXXXXXXXX
Cutis laxa, AD123700Graph: Cutis laxa, ADMouseHumanRatXXXXXXXXXX
Cutis laxa, autosomal dominant123700Graph: Cutis laxa, autosomal dominantMouseHumanRatXXXXXXXXXX
Cutis laxa, autosomal recessive219100Graph: Cutis laxa, autosomal recessiveXHumanRatXXXXXXXXXX
Cutis laxa, recessive, type I219100Graph: Cutis laxa, recessive, type IXHumanRatXXXXXXXXXX
Cyclic ichthyosis with epidermolytic hyperkeratosis607602Graph: Cyclic ichthyosis with epidermolytic hyperkeratosisMouseHumanXXXXXXXXXXX
Cylindromatosis, familial132700Graph: Cylindromatosis, familialXXXXXXXXXXXXX
Cystathioninuria219500Graph: CystathioninuriaMouseXXXXXXXXXYeastXX
Cystic fibrosis219700Graph: Cystic fibrosisMouseHumanRatXXXXXXXXXX
Cystic fibrosis lung disease, modifier of219700Graph: Cystic fibrosis lung disease, modifier ofMouseHumanRatXXXXXXXXXX
Cystinosis, late-onset juvenile or adolescent nephropathic219900Graph: Cystinosis, late-onset juvenile or adolescent nephropathicXHumanXXXXXXXXYeastXX
Cystinosis, nephropathic219800Graph: Cystinosis, nephropathicXHumanXXXXXXXXYeastXX
Cystinosis, ocular nonnephropathic219750Graph: Cystinosis, ocular nonnephropathicXHumanXXXXXXXXYeastXX
Cystinuria220100Graph: CystinuriaMouseHumanRatXXXXXXXYeastXX

D
OMIM disorder(s)OMIM_idComparisonGraphMouseHumanRatWormFlyDictyChickenZfinRiceTairYeastPombePfalc
D-bifunctional protein deficiency261515Graph: D-bifunctional protein deficiencyMouseHumanRatWormXDictyXXXXYeastXX
Dandy-Walker malformation220200Graph: Dandy-Walker malformationMouseHumanXWormXXChickenZfinXTairXXX
Darier disease124200Graph: Darier diseaseMouseHumanRatWormXXXXXXXXX
Deafness, X-linked 3, conductive, with stapes fixation304400Graph: Deafness, X-linked 3, conductive, with stapes fixationXHumanXXXXXXXXXXX
Deafness, autosomal dominant 1124900Graph: Deafness, autosomal dominant 1MouseHumanXWormXXXXXXYeastXX
Deafness, autosomal dominant 10601316Graph: Deafness, autosomal dominant 10XHumanXXXXXXXXXXX
Deafness, autosomal dominant 11, neurosensory601317Graph: Deafness, autosomal dominant 11, neurosensoryMouseHumanRatXXDictyXXXXXXX
Deafness, autosomal dominant 12601842Graph: Deafness, autosomal dominant 12MouseHumanXXXXXXXXXXX
Deafness, autosomal dominant 13601868Graph: Deafness, autosomal dominant 13XXXXXXXXXXXXX
Deafness, autosomal dominant 15602459Graph: Deafness, autosomal dominant 15MouseHumanXWormXXXZfinXXXXX
Deafness, autosomal dominant 17603622Graph: Deafness, autosomal dominant 17MouseXXWormXDictyXXXXYeastPombeX
Deafness, autosomal dominant 2600101Graph: Deafness, autosomal dominant 2MouseHumanRatXXXXXXXXXX
Deafness, autosomal dominant 20/26604717Graph: Deafness, autosomal dominant 20/26MouseHumanXWormXDictyXXRiceXYeastXX
Deafness, autosomal dominant 22606346Graph: Deafness, autosomal dominant 22MouseHumanXXXXXXXXXXX
Deafness, autosomal dominant 28608641Graph: Deafness, autosomal dominant 28XXXWormXXXXXXXXX
Deafness, autosomal dominant 3601544Graph: Deafness, autosomal dominant 3MouseHumanRatXXXXXXXXXX
Deafness, autosomal dominant 36606705Graph: Deafness, autosomal dominant 36MouseXXXXXXXXXXXX
Deafness, autosomal dominant 36, with dentinogenesis605594Graph: Deafness, autosomal dominant 36, with dentinogenesisXHumanRatXXXXXXXYeastXX
Deafness, autosomal dominant 4600652Graph: Deafness, autosomal dominant 4MouseXXWormXDictyXXXXYeastPombeX
Deafness, autosomal dominant 8601543Graph: Deafness, autosomal dominant 8MouseHumanXXXXXXXXXXX
Deafness, autosomal dominant 9601369Graph: Deafness, autosomal dominant 9XHumanXXXXXXXXXXX
Deafness, autosomal dominant nonsyndromic sensorineural607841Graph: Deafness, autosomal dominant nonsyndromic sensorineuralXHumanRatXXXXXXXXXX
Deafness, autosomal recessive 1220290Graph: Deafness, autosomal recessive 1MouseHumanRatXXXXXXXXXX
Deafness, autosomal recessive 10, congenital605316Graph: Deafness, autosomal recessive 10, congenitalXHumanXXXXXXXXXXX
Deafness, autosomal recessive 12601386Graph: Deafness, autosomal recessive 12MouseXRatXXXXXXXXXX
Deafness, autosomal recessive 16603720Graph: Deafness, autosomal recessive 16XXXXXXXXXXXXX
Deafness, autosomal recessive 18602092Graph: Deafness, autosomal recessive 18MouseXRatXXXXXXXXXX
Deafness, autosomal recessive 2, neurosensory600060Graph: Deafness, autosomal recessive 2, neurosensoryMouseHumanRatXXDictyXXXXXXX
Deafness, autosomal recessive 21603629Graph: Deafness, autosomal recessive 21MouseHumanXXXXXXXXXXX
Deafness, autosomal recessive 22607039Graph: Deafness, autosomal recessive 22MouseXXXXXXXXXXXX
Deafness, autosomal recessive 23609533Graph: Deafness, autosomal recessive 23MouseXXXXXXZfinXXXXX
Deafness, autosomal recessive 3600316Graph: Deafness, autosomal recessive 3MouseHumanXXXXXXXXXXX
Deafness, autosomal recessive 30607101Graph: Deafness, autosomal recessive 30XXXXXXXXXXXXX
Deafness, autosomal recessive 36609006Graph: Deafness, autosomal recessive 36MouseXRatXXXXXXXXXX
Deafness, autosomal recessive 37607821Graph: Deafness, autosomal recessive 37MouseHumanXXXXXXXXXXX
Deafness, autosomal recessive 4600791Graph: Deafness, autosomal recessive 4XHumanXXXXXXXXXXX
Deafness, autosomal recessive 6600971Graph: Deafness, autosomal recessive 6MouseXXXXXXXXXXXX
Deafness, autosomal recessive 7600974Graph: Deafness, autosomal recessive 7MouseXXXXXXXXXXXX
Deafness, autosomal recessive 8, childhood onset601072Graph: Deafness, autosomal recessive 8, childhood onsetXHumanXXXXXXXXXXX
Deafness, autosomal recessive 9601071Graph: Deafness, autosomal recessive 9XHumanXWormXXXXXXXXX
Deafness, sensorineural, with hypertrophic cardiomyopathy606346Graph: Deafness, sensorineural, with hypertrophic cardiomyopathyMouseHumanXXXXXXXXXXX
Dejerine-Sottas disease145900Graph: Dejerine-Sottas diseaseMouseHumanRatXXXXXXXYeastXX
Dejerine-Sottas neuropathy145900Graph: Dejerine-Sottas neuropathyMouseHumanRatXXXXXXXYeastXX
Dejerine-Sottas neuropathy, autosomal recessive145900Graph: Dejerine-Sottas neuropathy, autosomal recessiveMouseHumanRatXXXXXXXYeastXX
Dejerine-Sottas syndrome145900Graph: Dejerine-Sottas syndromeMouseHumanRatXXXXXXXYeastXX
Dementia, Lewy body127750Graph: Dementia, Lewy bodyMouseHumanRatXXXXXXXXXX
Dementia, Pick disease-like172700Graph: Dementia, Pick disease-likeMouseHumanRatXXXXXXXXXX
Dementia, familial British176500Graph: Dementia, familial BritishMouseHumanXXXXXXXXXXX
Dementia, familial Danish117300Graph: Dementia, familial DanishMouseHumanXXXXXXXXXXX
Dementia, frontotemporal600274Graph: Dementia, frontotemporalMouseHumanRatXXXXXXXXXX
Dementia, frontotemporal, with parkinsonism600274Graph: Dementia, frontotemporal, with parkinsonismMouseHumanRatXXXXXXXXXX
Dent disease300009Graph: Dent diseaseMouseHumanRatXXXXXXXYeastXX
Dentatorubro-pallidoluysian atrophy125370Graph: Dentatorubro-pallidoluysian atrophyXXRatWormXXXXXXXXX
Dentin dysplasia, type II125420Graph: Dentin dysplasia, type IIXHumanRatXXXXXXXYeastXX
Dentinogenesis imperfecta, Shields type II125490Graph: Dentinogenesis imperfecta, Shields type IIXHumanRatXXXXXXXYeastXX
Dentinogenesis imperfecta, Shields type III125500Graph: Dentinogenesis imperfecta, Shields type IIIXHumanRatXXXXXXXYeastXX
Denys-Drash syndrome194080Graph: Denys-Drash syndromeMouseXXXXXXXXXXXX
Desmoid disease, hereditary135290Graph: Desmoid disease, hereditaryMouseHumanRatWormFlyXXXXXXXX
Desmosterolosis602398Graph: DesmosterolosisMouseXXXXXXXXXXXX
DiGeorge syndrome188400Graph: DiGeorge syndromeXHumanXWormXXXXXXXXX
Diabetes insipidus, nephrogenic125800Graph: Diabetes insipidus, nephrogenicMouseHumanRatXXXXXXXYeastXX
Diabetes insipidus, neurohypophyseal125700Graph: Diabetes insipidus, neurohypophysealXHumanRatXXXXXXXXXX
Diabetes mellitus, gestational125851Graph: Diabetes mellitus, gestationalMouseHumanRatXXXXXXXYeastXX
Diabetes mellitus, insulin-resistant, with acanthosis nigricans and hypertension604367Graph: Diabetes mellitus, insulin-resistant, with acanthosis nigricans and hypertensionMouseHumanRatXXXXXXXXXX
Diabetes mellitus, noninsulin-dependent125853Graph: Diabetes mellitus, noninsulin-dependentMouseHumanRatWormFlyDictyXZfinXXYeastXX
Diabetes mellitus, noninsulin-dependent, late onset125853Graph: Diabetes mellitus, noninsulin-dependent, late onsetMouseHumanRatWormFlyDictyXZfinXXYeastXX
Diabetes mellitus, permanent neonatal606176Graph: Diabetes mellitus, permanent neonatalMouseHumanRatXXXXXXXYeastXX
Diabetes mellitus, permanent neonatal, with neurologic features606176Graph: Diabetes mellitus, permanent neonatal, with neurologic featuresMouseHumanRatXXXXXXXYeastXX
Diabetes mellitus, type II125853Graph: Diabetes mellitus, type IIMouseHumanRatWormFlyDictyXZfinXXYeastXX
Diabetes, permanent neonatal606176Graph: Diabetes, permanent neonatalMouseHumanRatXXXXXXXYeastXX
Diastrophic dysplasia222600Graph: Diastrophic dysplasiaXHumanRatXXXXXXXXXX
Dicarboxylicaminoaciduria222730Graph: DicarboxylicaminoaciduriaMouseHumanXXXXXXXXXXX
Dilated cardiomyopathy with woolly hair and keratoderma605676Graph: Dilated cardiomyopathy with woolly hair and keratodermaXHumanXXXXXXXXXXX
Dimethylglycine dehydrogenase deficiency605850Graph: Dimethylglycine dehydrogenase deficiencyMouseHumanRatXXXXXXXXXX
Disordered steroidogenesis, isolated201750Graph: Disordered steroidogenesis, isolatedMouseHumanXXXXXXXXYeastXX
Dosage-sensitive sex reversal300018Graph: Dosage-sensitive sex reversalMouseXXXXXXXXXXXX
Double-outlet right ventricle217095Graph: Double-outlet right ventricleXHumanXWormXXXXXXXXX
Dowling-Degos disease179850Graph: Dowling-Degos diseaseMouseHumanXXXXXXXXXXX
Doyne honeycomb degeneration of retina126600Graph: Doyne honeycomb degeneration of retinaXHumanXXXXXXXXXXX
Duane-radial ray syndrome607323Graph: Duane-radial ray syndromeXXXWormXXXXXXXXX
Dubin-Johnson syndrome237500Graph: Dubin-Johnson syndromeMouseHumanRatXXXXXXXYeastXX
Duchenne muscular dystrophy310200Graph: Duchenne muscular dystrophyMouseHumanXWormXXXZfinXXXXX
Dyggve-Melchior-Clausen disease223800Graph: Dyggve-Melchior-Clausen diseaseXXXXXXXXXXXXX
Dysautonomia, familial223900Graph: Dysautonomia, familialXHumanXXXXXXXXYeastXX
Dyschromatosis symmetrica hereditaria127400Graph: Dyschromatosis symmetrica hereditariaMouseHumanRatXXXXXXXYeastXX
Dyserythropoietic anemia with thrombocytopenia300367Graph: Dyserythropoietic anemia with thrombocytopeniaMouseHumanRatXXXXXXXXXX
Dyskeratosis congenita-1305000Graph: Dyskeratosis congenita-1XHumanRatXXXXXXXYeastXX
Dyssegmental dysplasia, Silverman-Handmaker type224410Graph: Dyssegmental dysplasia, Silverman-Handmaker typeMouseXXWormXXXXXXXXX
Dystonia, DOPA-responsive128230Graph: Dystonia, DOPA-responsiveXHumanRatXXDictyXXXXYeastXX
Dystonia, myoclonic159900Graph: Dystonia, myoclonicMouseHumanRatXXXXXXXXXX
Dystonia-1, torsion128100Graph: Dystonia-1, torsionXHumanRatXXXXXXXXXX

E
OMIM disorder(s)OMIM_idComparisonGraphMouseHumanRatWormFlyDictyChickenZfinRiceTairYeastPombePfalc
EBD, Bart type132000Graph: EBD, Bart typeXHumanXXXXXXXXXXX
Ectodermal dysplasia 2, hidrotic129500Graph: Ectodermal dysplasia 2, hidroticMouseHumanRatXXXXXXXXXX
Ectodermal dysplasia, Margarita Island type225060Graph: Ectodermal dysplasia, Margarita Island typeMouseHumanXXXXXXXXXXX
Ectodermal dysplasia, hypohidrotic, autosomal dominant129490Graph: Ectodermal dysplasia, hypohidrotic, autosomal dominantMouseHumanXXXXXXXXXXX
Ectodermal dysplasia, hypohidrotic, autosomal recessive224900Graph: Ectodermal dysplasia, hypohidrotic, autosomal recessiveMouseHumanXXXXXXXXXXX
Ectodermal dysplasia, hypohidrotic, with immune deficiency300291Graph: Ectodermal dysplasia, hypohidrotic, with immune deficiencyMouseHumanRatXXXXXXXXXX
Ectodermal dysplasia-1, anhidrotic305100Graph: Ectodermal dysplasia-1, anhidroticMouseHumanXXXXXXXXXXX
Ectodermal dysplasia/skin fragility syndrome604536Graph: Ectodermal dysplasia/skin fragility syndromeMouseHumanXXXXXXXXXXX
Ectodermal, dysplasia, anhidrotic, lymphedema and immunodeficiency300301Graph: Ectodermal, dysplasia, anhidrotic, lymphedema and immunodeficiencyMouseHumanRatXXXXXXXXXX
Ectopia lentis, familial129600Graph: Ectopia lentis, familialMouseHumanXWormXXXXXXXXX
Ectopia pupillae129750Graph: Ectopia pupillaeMouseHumanRatWormXXChickenXXXYeastXX
Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3604292Graph: Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3MouseHumanRatXXXXXXXXXX
Ehlers-Danlos due to tenascin X deficiency606408Graph: Ehlers-Danlos due to tenascin X deficiencyMouseXXXFlyXXXXXXXX
Ehlers-Danlos syndrome, hypermobility type130020Graph: Ehlers-Danlos syndrome, hypermobility typeMouseHumanXXFlyXXXXXXXX
Ehlers-Danlos syndrome, progeroid form130070Graph: Ehlers-Danlos syndrome, progeroid formXHumanXWormXXXXXXXXX
Ehlers-Danlos syndrome, type I130000Graph: Ehlers-Danlos syndrome, type IMouseHumanRatXXXXXXXXXX
Ehlers-Danlos syndrome, type II130010Graph: Ehlers-Danlos syndrome, type IIXHumanRatXXXXXXXXXX
Ehlers-Danlos syndrome, type III130020Graph: Ehlers-Danlos syndrome, type IIIMouseHumanXXFlyXXXXXXXX
Ehlers-Danlos syndrome, type IV130050Graph: Ehlers-Danlos syndrome, type IVXHumanXXXXXXXXXXX
Ehlers-Danlos syndrome, type VI225400Graph: Ehlers-Danlos syndrome, type VIXHumanXWormXXXXXXXXX
Ehlers-Danlos syndrome, type VII130060Graph: Ehlers-Danlos syndrome, type VIIXHumanXXXXXXXXXXX
Ehlers-Danlos syndrome, type VIIA2130060Graph: Ehlers-Danlos syndrome, type VIIA2XHumanXXXXXXXXXXX
Ehlers-Danlos syndrome, type VIIC225410Graph: Ehlers-Danlos syndrome, type VIICXHumanXXXXXXXXXXX
Ehlers-Danlos syndrome, type X225310Graph: Ehlers-Danlos syndrome, type XMouseHumanRatXXXXZfinXXXXX
Ellis-van Creveld syndrome225500Graph: Ellis-van Creveld syndromeXHumanXXXXXXXXXXX
Emery-Dreifuss muscular dystrophy310300Graph: Emery-Dreifuss muscular dystrophyMouseHumanXXXXXXXXXXX
Emery-Dreifuss muscular dystrophy, AD181350Graph: Emery-Dreifuss muscular dystrophy, ADMouseHumanRatWormXXXXXXXXX
Emery-Dreifuss muscular dystrophy, AR604929Graph: Emery-Dreifuss muscular dystrophy, ARMouseHumanRatWormXXXXXXXXX
Encephalopathy, familial, with neuroserpin inclusion bodies604218Graph: Encephalopathy, familial, with neuroserpin inclusion bodiesXHumanXXXXXXXXXXX
Enchondromatosis, Ollier type166000Graph: Enchondromatosis, Ollier typeMouseHumanRatXXXXXXXXXX
Enhanced S-cone syndrome268100Graph: Enhanced S-cone syndromeMouseHumanXXXXXXXXXXX
Enlarged vestibular aqueduct603545Graph: Enlarged vestibular aqueductXHumanXXXXXXXXXXX
Enterokinase deficiency226200Graph: Enterokinase deficiencyXHumanXXXXXXXXXXX
Eosinophil peroxidase deficiency261500Graph: Eosinophil peroxidase deficiencyXHumanXXXXXZfinXXXXX
Epidermodysplasia verruciformis226400Graph: Epidermodysplasia verruciformisXXXXXXXXXXXXX
Epidermolysis bullosa dystrophica, AD131750Graph: Epidermolysis bullosa dystrophica, ADXHumanXXXXXXXXXXX
Epidermolysis bullosa dystrophica, AR226600Graph: Epidermolysis bullosa dystrophica, ARXHumanXXXXXXXXXXX
Epidermolysis bullosa of hands and feet131800Graph: Epidermolysis bullosa of hands and feetMouseHumanRatXXXXXXXXXX
Epidermolysis bullosa pruriginosa604129Graph: Epidermolysis bullosa pruriginosaXHumanXXXXXXXXXXX
Epidermolysis bullosa simplex with mottled pigmentation131960Graph: Epidermolysis bullosa simplex with mottled pigmentationMouseHumanXXXXXXXXXXX
Epidermolysis bullosa simplex, Koebner, Dowling-Meara, and Weber-Cockayne types131800Graph: Epidermolysis bullosa simplex, Koebner, Dowling-Meara, and Weber-Cockayne typesMouseHumanRatXXXXXXXXXX
Epidermolysis bullosa simplex, Ogna type131950Graph: Epidermolysis bullosa simplex, Ogna typeMouseHumanRatXXDictyXXXXXXX
Epidermolysis bullosa simplex, recessive601001Graph: Epidermolysis bullosa simplex, recessiveMouseHumanXXXXXXXXXXX
Epidermolysis bullosa, Herlitz junctional type226700Graph: Epidermolysis bullosa, Herlitz junctional typeMouseHumanRatXXXXXXXXXX
Epidermolysis bullosa, generalized atrophic benign226650Graph: Epidermolysis bullosa, generalized atrophic benignMouseHumanRatXXXXXXXXXX
Epidermolysis bullosa, junctional, Herlitz type226700Graph: Epidermolysis bullosa, junctional, Herlitz typeMouseHumanRatXXXXXXXXXX
Epidermolysis bullosa, junctional, with pyloric atresia226730Graph: Epidermolysis bullosa, junctional, with pyloric atresiaMouseHumanRatWormXXXXXXXXX
Epidermolysis bullosa, junctional, with pyloric stenosis226730Graph: Epidermolysis bullosa, junctional, with pyloric stenosisMouseHumanRatWormXXXXXXXXX
Epidermolysis bullosa, lethal acantholytic609638Graph: Epidermolysis bullosa, lethal acantholyticXHumanXXXXXXXXXXX
Epidermolysis bullosa, pretibial131850Graph: Epidermolysis bullosa, pretibialXHumanXXXXXXXXXXX
Epidermolytic hyperkeratosis113800Graph: Epidermolytic hyperkeratosisMouseHumanXXXXXXXXXXX
Epidermolytic palmoplantar keratoderma144200Graph: Epidermolytic palmoplantar keratodermaMouseHumanRatXXXXXXXXXX
Epilepsy with grand mal seizures on awakening607628Graph: Epilepsy with grand mal seizures on awakeningXHumanRatXXXXXXXXXX
Epilepsy, X-linked, with variable learning disabilities and behavior disorders300491Graph: Epilepsy, X-linked, with variable learning disabilities and behavior disordersMouseHumanRatXXXXXXXXXX
Epilepsy, benign neonatal, type 2121201Graph: Epilepsy, benign neonatal, type 2XHumanXXXXXXXXXXX
Epilepsy, benign, neonatal, type 1121200Graph: Epilepsy, benign, neonatal, type 1XHumanXXXXXXXXXXX
Epilepsy, childhood absence607681Graph: Epilepsy, childhood absenceMouseHumanRatXXXXXXXXXX
Epilepsy, generalized idiopathic600669Graph: Epilepsy, generalized idiopathicMouseHumanXWormXXXXXXXXX
Epilepsy, generalized, with febrile seizures plus604233Graph: Epilepsy, generalized, with febrile seizures plusMouseHumanRatXXXXXXXXXX
Epilepsy, generalized, with febrile seizures plus, type 2604233Graph: Epilepsy, generalized, with febrile seizures plus, type 2MouseHumanRatXXXXXXXXXX
Epilepsy, intractable childhood, with generalized tonic-clonic seiqures607208Graph: Epilepsy, intractable childhood, with generalized tonic-clonic seiquresMouseHumanRatXXXXXXXXXX
Epilepsy, juvenile absence607631Graph: Epilepsy, juvenile absenceXHumanRatXXXXXXXXXX
Epilepsy, juvenile myoclonic606904Graph: Epilepsy, juvenile myoclonicMouseHumanRatWormXXXXXXXXX
Epilepsy, myoclonic, Lafora type254780Graph: Epilepsy, myoclonic, Lafora typeMouseHumanXXXDictyXXXXXXX
Epilepsy, nocturnal frontal lobe, 1600513Graph: Epilepsy, nocturnal frontal lobe, 1MouseHumanRatWormXXXXXXXXX
Epilepsy, nocturnal frontal lobe, 3605375Graph: Epilepsy, nocturnal frontal lobe, 3MouseHumanRatXXXXXXXXXX
Epilepsy, partial, with auditory features600512Graph: Epilepsy, partial, with auditory featuresXHumanXXXXXXXXXXX
Epilepsy, progressive myoclonic 1254800Graph: Epilepsy, progressive myoclonic 1MouseXRatXXDictyXXXXXXX
Epilepsy, progressive myoclonic 2B254780Graph: Epilepsy, progressive myoclonic 2BMouseHumanXXXDictyXXXXXXX
Epilepsy, severe myoclonic, of infancy607208Graph: Epilepsy, severe myoclonic, of infancyMouseHumanRatXXXXXXXXXX
Epiphyseal dysplasia, multiple 1132400Graph: Epiphyseal dysplasia, multiple 1XHumanXXXXXXXXXXX
Epiphyseal dysplasia, multiple, 2600204Graph: Epiphyseal dysplasia, multiple, 2XHumanXXXXXXXXXXX
Epiphyseal dysplasia, multiple, 3600969Graph: Epiphyseal dysplasia, multiple, 3XHumanXXXXXXXXXXX
Epiphyseal dysplasia, multiple, 4226900Graph: Epiphyseal dysplasia, multiple, 4XHumanRatXXXXXXXXXX
Epiphyseal dysplasia, multiple, 5607078Graph: Epiphyseal dysplasia, multiple, 5MouseHumanXXXXXXXXXXX
Episodic ataxia, type 2108500Graph: Episodic ataxia, type 2MouseHumanRatXXXXXXXXXX
Episodic ataxia/myokymia syndrome160120Graph: Episodic ataxia/myokymia syndromeXHumanRatXXXXXXXXXX
Epstein syndrome153650Graph: Epstein syndromeMouseXXWormXDictyXXXXYeastPombeX
Erythermalgia, primary133020Graph: Erythermalgia, primaryXHumanXXXXXXXXXXX
Erythrokeratodermia variabilis133200Graph: Erythrokeratodermia variabilisMouseXRatXXXXXXXXXX
Erythrokeratodermia variabilis with erythema gyratum repens133200Graph: Erythrokeratodermia variabilis with erythema gyratum repensMouseXRatXXXXXXXXXX
Esophageal cancer133239Graph: Esophageal cancerMouseHumanRatXXXXXXXXXX
Esophageal carcinoma, somatic133239Graph: Esophageal carcinoma, somaticMouseHumanRatXXXXXXXXXX
Esophageal squamous cell carcinoma133239Graph: Esophageal squamous cell carcinomaMouseHumanRatXXXXXXXXXX
Ethylmalonic encephalopathy602473Graph: Ethylmalonic encephalopathyMouseXXXXXXXXXXXX
Exostoses, multiple, type 1133700Graph: Exostoses, multiple, type 1MouseHumanXXXXXXXXXXX
Exostoses, multiple, type 2133701Graph: Exostoses, multiple, type 2XHumanXXXXXXXXXXX
Exudative vitreoretinopathy133780Graph: Exudative vitreoretinopathyMouseHumanXXXDictyXXXXXXX
Exudative vitreoretinopathy, X-linked305390Graph: Exudative vitreoretinopathy, X-linkedXHumanXXXXXXXXXXX
Exudative vitreoretinopathy, dominant133780Graph: Exudative vitreoretinopathy, dominantMouseHumanXXXDictyXXXXXXX
Exudative vitreoretinopathy, recessive601813Graph: Exudative vitreoretinopathy, recessiveMouseHumanXXXDictyXXXXXXX

F
OMIM disorder(s)OMIM_idComparisonGraphMouseHumanRatWormFlyDictyChickenZfinRiceTairYeastPombePfalc
Factor V and factor VIII, combined deficiency of227300Graph: Factor V and factor VIII, combined deficiency ofMouseHumanXXXXXXXXXXX
Familial Mediterranean fever249100Graph: Familial Mediterranean feverXHumanXXXXXXXXXXX
Fanconi anemia, complementation group D1605724Graph: Fanconi anemia, complementation group D1MouseHumanRatXXXXXXXXXX
Fanconi anemia, complementation group J609054Graph: Fanconi anemia, complementation group JXHumanXWormXXXXXXXXX
Fanconi-Bickel syndrome227810Graph: Fanconi-Bickel syndromeMouseHumanRatXXXXXXXYeastXX
Febrile convulsions, familial, 3604403Graph: Febrile convulsions, familial, 3XXRatXXXXXXXXXX
Fechtner syndrome153640Graph: Fechtner syndromeMouseXXWormXDictyXXXXYeastPombeX
Fertile eunuch syndrome228300Graph: Fertile eunuch syndromeXHumanRatXXXXXXXXXX
Fibromatosis, gingival135300Graph: Fibromatosis, gingivalXHumanXWormXDictyXXXXXXX
Fibromatosis, juvenile hyaline228600Graph: Fibromatosis, juvenile hyalineXHumanXXXXXXXXXXX
Fibrosis of extraocular muscles, congenital, 1135700Graph: Fibrosis of extraocular muscles, congenital, 1XXXXXXXXXXXXX
Fibrosis of extraocular muscles, congenital, 2602078Graph: Fibrosis of extraocular muscles, congenital, 2MouseXRatXXXXXXXXXX
Fibular hypoplasia and complex brachydactyly228900Graph: Fibular hypoplasia and complex brachydactylyMouseHumanXXXXXXXXXXX
Fish-eye disease136120Graph: Fish-eye diseaseXHumanXXXXXXXXYeastXX
Focal cortical dysplasia, Taylor balloon cell type607341Graph: Focal cortical dysplasia, Taylor balloon cell typeXHumanRatXXXXXXXXXX
Follicle-stimulating hormone deficiency, isolated229070Graph: Follicle-stimulating hormone deficiency, isolatedXHumanXXXXXXXXXXX
Foveal hypoplasia, isolated136520Graph: Foveal hypoplasia, isolatedMouseHumanRatWormXXChickenXXXYeastXX
Foveomacular dystrophy, adult-onset, with choroidal neovascularization608161Graph: Foveomacular dystrophy, adult-onset, with choroidal neovascularizationXHumanXXXXXXXXXXX
Fraser syndrome219000Graph: Fraser syndromeMouseXXXXXXXXXXXX
Frasier syndrome136680Graph: Frasier syndromeMouseXXXXXXXXXXXX
Friedreich ataxia229300Graph: Friedreich ataxiaMouseXXWormXXXXXXYeastXX
Friedreich ataxia with retained reflexes229300Graph: Friedreich ataxia with retained reflexesMouseXXWormXXXXXXYeastXX
Frontometaphyseal dysplasia304120Graph: Frontometaphyseal dysplasiaMouseHumanXXXDictyXXXXXXX
Fumarase deficiency606812Graph: Fumarase deficiencyMouseHumanXWormXXXXXXYeastXX
Fundus albipunctatus136880Graph: Fundus albipunctatusMouseHumanXXXXXXXXXXX
Fundus flavimaculatus248200Graph: Fundus flavimaculatusMouseHumanXXXXXXXXXXX

G
OMIM disorder(s)OMIM_idComparisonGraphMouseHumanRatWormFlyDictyChickenZfinRiceTairYeastPombePfalc
GM2-gangliosidosis, several forms272800Graph: GM2-gangliosidosis, several formsMouseHumanXXXXXXXXXXX
GRACILE syndrome603358Graph: GRACILE syndromeXHumanXXXXXXXXYeastXX
Galactokinase deficiency with cataracts230200Graph: Galactokinase deficiency with cataractsMouseHumanXXXXXXXXXXX
Galactose epimerase deficiency230350Graph: Galactose epimerase deficiencyMouseXXXXXXXXXYeastXX
Galactosemia230400Graph: GalactosemiaMouseHumanXXXXXXXXYeastXX
Gallbladder disease 1600803Graph: Gallbladder disease 1MouseHumanXWormXDictyXXXXYeastXPfalc
Gastric cancer137215Graph: Gastric cancerMouseHumanRatWormFlyDictyXXXXXXX
Gastric cancer, familial diffuse137215Graph: Gastric cancer, familial diffuseMouseHumanRatWormFlyDictyXXXXXXX
Gastric cancer, somatic137215Graph: Gastric cancer, somaticMouseHumanRatWormFlyDictyXXXXXXX
Gastrointestinal stromal tumor, somatic606764Graph: Gastrointestinal stromal tumor, somaticMouseHumanRatXXXXXXXXXX
Gaucher disease230800Graph: Gaucher diseaseXXXXXXXXXXXXX
Gaucher disease with cardiovascular calcification231005Graph: Gaucher disease with cardiovascular calcificationXXXXXXXXXXXXX
Generalized epilepsy with febrile seizures plus604233Graph: Generalized epilepsy with febrile seizures plusMouseHumanRatXXXXXXXXXX
Germ cell tumors273300Graph: Germ cell tumorsMouseHumanRatXXXXXXXXXX
Gerstmann-Straussler disease137440Graph: Gerstmann-Straussler diseaseMouseHumanRatXXXXXXXXXX
Giant axonal neuropathy-1256850Graph: Giant axonal neuropathy-1XHumanXXXXXXXXXXX
Giant cell hepatitis, neonatal231100Graph: Giant cell hepatitis, neonatalXHumanXXXXXXXXXXX
Gitelman syndrome263800Graph: Gitelman syndromeXHumanXXXXXXXXXXX
Glaucoma 1A, primary open angle, juvenile-onset137750Graph: Glaucoma 1A, primary open angle, juvenile-onsetMouseHumanRatXXXXXXXXXX
Glaucoma 1E, primary open angle, adult-onset137760Graph: Glaucoma 1E, primary open angle, adult-onsetXHumanRatXXXXXXXXXX
Glaucoma 3A, primary congenital231300Graph: Glaucoma 3A, primary congenitalXHumanRatXXXXXXXXXX
Glaucoma, primary open angle, adult-onset137760Graph: Glaucoma, primary open angle, adult-onsetXHumanRatXXXXXXXXXX
Glaucoma, primary open angle, juvenile-onset137750Graph: Glaucoma, primary open angle, juvenile-onsetMouseHumanRatXXXXXXXXXX
Glioblastoma137800Graph: GlioblastomaMouseHumanRatWormXDictyXXXXXXX
Glioblastoma multiforme, somatic137800Graph: Glioblastoma multiforme, somaticMouseHumanRatWormXDictyXXXXXXX
Glioblastoma, somatic137800Graph: Glioblastoma, somaticMouseHumanRatWormXDictyXXXXXXX
Globozoospermia102530Graph: GlobozoospermiaMouseXXXXXXXXXXXX
Glomerulocystic kidney disease with hyperuricemia and isosthenuria609886Graph: Glomerulocystic kidney disease with hyperuricemia and isosthenuriaXHumanRatXXXXXXXXXX
Glomerulosclerosis, focal segmental, 1603278Graph: Glomerulosclerosis, focal segmental, 1MouseHumanRatWormXDictyXXXXXXX
Glomerulosclerosis, focal segmental, 3607832Graph: Glomerulosclerosis, focal segmental, 3MouseHumanRatXXXXXXXYeastXX
Glomuvenous malformations138000Graph: Glomuvenous malformationsXXXXXXXXXXXXX
Glucocorticoid deficiency, due to ACTH unresponsiveness202200Graph: Glucocorticoid deficiency, due to ACTH unresponsivenessXHumanXXXXXXXXXXX
Glucose transport defect, blood-brain barrier606777Graph: Glucose transport defect, blood-brain barrierMouseHumanRatXXXXXXXYeastXX
Glucose/galactose malabsorption606824Graph: Glucose/galactose malabsorptionMouseHumanRatXXXXXXXXXX
Glucosidase I deficiency606056Graph: Glucosidase I deficiencyXHumanXXXXXXXXYeastXX
Glutamate formiminotransferase deficiency229100Graph: Glutamate formiminotransferase deficiencyMouseHumanRatXXXXXXXXXX
Glutaricaciduria, type I231670Graph: Glutaricaciduria, type IMouseHumanXXXXXXXXXXX
Glutaricaciduria, type IIA231680Graph: Glutaricaciduria, type IIAMouseHumanXWormXXXXXXXXX
Glutaricaciduria, type IIB231680Graph: Glutaricaciduria, type IIBMouseHumanXWormXXXXXXXXX
Glutaricaciduria, type IIC231680Graph: Glutaricaciduria, type IICMouseHumanXWormXXXXXXXXX
Glutathione synthetase deficiency266130Graph: Glutathione synthetase deficiencyXHumanXXXXXXXXYeastXX
Glycerol kinase deficiency307030Graph: Glycerol kinase deficiencyXXXXXXXXXXYeastXX
Glycine N-methyltransferase deficiency606664Graph: Glycine N-methyltransferase deficiencyXXRatXXXXXXXXXX
Glycine encephalopathy605899Graph: Glycine encephalopathyXHumanXXXXXXXXYeastXX
Glycogen storage disease II232300Graph: Glycogen storage disease IIMouseHumanXXXXXXXXXXX
Glycogen storage disease IIb300257Graph: Glycogen storage disease IIbMouseHumanXWormXXXXXXXXX
Glycogen storage disease IV232500Graph: Glycogen storage disease IVXHumanXXXXXXXXYeastXX
Glycogen storage disease Ib232220Graph: Glycogen storage disease IbXXXXXXXXXXXXX
Glycogen storage disease Ic232240Graph: Glycogen storage disease IcXXXXXXXXXXXXX
Glycogen storage disease, type 0240600Graph: Glycogen storage disease, type 0XHumanXWormXXXXXXYeastXX
Gonadal dysgenesis, 46XY, partial, with minifascicular neuropathy607080Graph: Gonadal dysgenesis, 46XY, partial, with minifascicular neuropathyMouseXXWormXXXXXXXXX
Greenberg dysplasia215140Graph: Greenberg dysplasiaMouseHumanXXXXXXXXYeastXX
Greig cephalopolysyndactyly syndrome175700Graph: Greig cephalopolysyndactyly syndromeMouseHumanRatXFlyXXXXXYeastXX
Griscelli syndrome, type 1214450Graph: Griscelli syndrome, type 1MouseXRatXXXXXXXYeastXX
Griscelli syndrome, type 2607624Graph: Griscelli syndrome, type 2MouseHumanXWormXXXXXXXXX
Growth hormone insensitivity with immunodeficiency245590Graph: Growth hormone insensitivity with immunodeficiencyMouseHumanRatXXXXXXXXXX
Growth retardation with deafness and mental retardation due to IGF1 deficiency608747Graph: Growth retardation with deafness and mental retardation due to IGF1 deficiencyMouseHumanRatXXXXZfinXXXXX
Guttmacher syndrome176305Graph: Guttmacher syndromeMouseHumanXXXXXXXXXXX

H
OMIM disorder(s)OMIM_idComparisonGraphMouseHumanRatWormFlyDictyChickenZfinRiceTairYeastPombePfalc
HARP syndrome607236Graph: HARP syndromeXXXXXXXXXXXXX
HDL deficiency, familial604091Graph: HDL deficiency, familialMouseHumanRatXXXXXXXXXX
HMG-CoA synthase-2 deficiency605911Graph: HMG-CoA synthase-2 deficiencyMouseHumanRatXXXXXXXYeastXX
HPRT-related gout300323Graph: HPRT-related goutMouseHumanXXXXXXXXXXX
Hailey-Hailey disease169600Graph: Hailey-Hailey diseaseMouseHumanXXXXXXXXYeastXX
Haim-Munk syndrome245010Graph: Haim-Munk syndromeXHumanRatXXXXXXXXXX
Hand-foot-uterus syndrome140000Graph: Hand-foot-uterus syndromeMouseHumanXXXXXXXXXXX
Hartnup disorder234500Graph: Hartnup disorderMouseXRatXXXXXXXXXX
Hay-Wells syndrome106260Graph: Hay-Wells syndromeMouseHumanRatXXXXXXXXXX
Hearing loss, low-frequency sensorineural600965Graph: Hearing loss, low-frequency sensorineuralXHumanXXXXXXXXXXX
Heart block, nonprogressive113900Graph: Heart block, nonprogressiveXHumanRatXXXXXXXXXX
Heart block, progressive, type I113900Graph: Heart block, progressive, type IXHumanRatXXXXXXXXXX
Hemangioma, capillary infantile, somatic602089Graph: Hemangioma, capillary infantile, somaticMouseHumanRatWormXXXXXXXXX
Hematopoiesis, cyclic162800Graph: Hematopoiesis, cyclicXHumanXXXXXXXXXXX
Hemiplegic migraine, familial141500Graph: Hemiplegic migraine, familialMouseHumanRatXXXXXXXXXX
Hemochromatosis, juvenile602390Graph: Hemochromatosis, juvenileMouseHumanXXXXXXXXXXX
Hemochromatosis, juvenile, digenic602390Graph: Hemochromatosis, juvenile, digenicMouseHumanXXXXXXXXXXX
Hemochromatosis, type 2A602390Graph: Hemochromatosis, type 2AMouseHumanXXXXXXXXXXX
Hemochromatosis, type 3604250Graph: Hemochromatosis, type 3XHumanXXXXXXXXXXX
Hemochromatosis, type 4606069Graph: Hemochromatosis, type 4MouseHumanXXXXXXXXXXX
Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency230450Graph: Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiencyMouseHumanXXXXXXXXYeastXX
Hemolytic anemia due to glutathione synthetase deficiency231900Graph: Hemolytic anemia due to glutathione synthetase deficiencyXHumanXXXXXXXXYeastXX
Hemolytic-uremic syndrome235400Graph: Hemolytic-uremic syndromeXHumanRatXXXXXXXXXX
Hemophagocytic lymphohistiocytosis, familial, 2603553Graph: Hemophagocytic lymphohistiocytosis, familial, 2MouseHumanRatXXXXXXXXXX
Hemophagocytic lymphohistiocytosis, familial, 3608898Graph: Hemophagocytic lymphohistiocytosis, familial, 3XHumanRatXXXXXXXXXX
Hemosiderosis, systemic, due to aceruloplasminemia604290Graph: Hemosiderosis, systemic, due to aceruloplasminemiaXHumanRatXXXXXXXXXX
Hepatic adenoma142330Graph: Hepatic adenomaMouseHumanRatXXXXXXXXXX
Hepatocellular cancer114550Graph: Hepatocellular cancerMouseHumanRatWormXXXZfinXXXXX
Hepatocellular carcinoma114550Graph: Hepatocellular carcinomaMouseHumanRatWormXXXZfinXXXXX
Hepatocellular carcinoma, childhood type114550Graph: Hepatocellular carcinoma, childhood typeMouseHumanRatWormXXXZfinXXXXX
Hepatocellular carcinoma, somatic114550Graph: Hepatocellular carcinoma, somaticMouseHumanRatWormXXXZfinXXXXX
Hereditary hemorrhagic telangiectasia-1187300Graph: Hereditary hemorrhagic telangiectasia-1MouseHumanXXXXXXXXXXX
Hereditary hemorrhagic telangiectasia-2600376Graph: Hereditary hemorrhagic telangiectasia-2MouseHumanXXXXXXXXXXX
Hereditary motor and sensory neuropathy VI601152Graph: Hereditary motor and sensory neuropathy VIMouseHumanXWormXXXXXXXXX
Hermansky-Pudlak syndrome 1203300Graph: Hermansky-Pudlak syndrome 1MouseHumanXXXXXXXXXXX
Hermansky-Pudlak syndrome 2608233Graph: Hermansky-Pudlak syndrome 2MouseHumanXXXXXXXXYeastXX
Hermansky-Pudlak syndrome 3203300Graph: Hermansky-Pudlak syndrome 3MouseHumanXXXXXXXXXXX
Hermansky-Pudlak syndrome 4203300Graph: Hermansky-Pudlak syndrome 4MouseHumanXXXXXXXXXXX
Hermansky-Pudlak syndrome 6203300Graph: Hermansky-Pudlak syndrome 6MouseHumanXXXXXXXXXXX
Hermansky-Pudlak syndrome 7203300Graph: Hermansky-Pudlak syndrome 7MouseHumanXXXXXXXXXXX
Hermansky-pudlak syndrome 5203300Graph: Hermansky-pudlak syndrome 5MouseHumanXXXXXXXXXXX
Heterotaxy, X-linked visceral306955Graph: Heterotaxy, X-linked visceralMouseHumanXWormXXXZfinXTairXXX
Heterotaxy, visceral605376Graph: Heterotaxy, visceralXXXXXXXXXXXXX
Heterotopia, periventricular300049Graph: Heterotopia, periventricularMouseHumanXXXDictyXXXXXXX
Heterotopia, periventricular nodular, with frontometaphyseal dysplasia300049Graph: Heterotopia, periventricular nodular, with frontometaphyseal dysplasiaMouseHumanXXXDictyXXXXXXX
Heterotopia, periventricular, ED variant300537Graph: Heterotopia, periventricular, ED variantMouseHumanXXXDictyXXXXXXX
Hirschsprung disease142623Graph: Hirschsprung diseaseMouseHumanRatXXXXZfinXXXXX
Hirschsprung disease, short-segment142623Graph: Hirschsprung disease, short-segmentMouseHumanRatXXXXZfinXXXXX
Hirschsprung disease-2600155Graph: Hirschsprung disease-2MouseHumanRatXXXXXXXXXX
Holoprosencephaly-2157170Graph: Holoprosencephaly-2MouseHumanXWormXXXXXXXXX
Holoprosencephaly-3142945Graph: Holoprosencephaly-3MouseHumanRatWormXXXXXXXXX
Holoprosencephaly-4142946Graph: Holoprosencephaly-4XHumanXXXXXXXXXXX
Holoprosencephaly-5609637Graph: Holoprosencephaly-5MouseHumanXWormXXXXXTairXXX
Holt-Oram syndrome142900Graph: Holt-Oram syndromeMouseHumanXXXXXXXXXXX
Homocystinuria due to MTHFR deficiency236250Graph: Homocystinuria due to MTHFR deficiencyMouseHumanXXXXXXXXYeastXX
Homocystinuria-megaloblastic anemia, cbl E type236270Graph: Homocystinuria-megaloblastic anemia, cbl E typeXXXXXXXXXXXXX
Homozygous 2p16 deletion syndrome606407Graph: Homozygous 2p16 deletion syndromeMouseHumanRatXXXXXXXYeastXX
Hoyeraal-Hreidarsson syndrome300240Graph: Hoyeraal-Hreidarsson syndromeXHumanRatXXXXXXXYeastXX
Huntington disease-like 1603218Graph: Huntington disease-like 1MouseHumanRatXXXXXXXXXX
Huntington disease-like 2606438Graph: Huntington disease-like 2MouseXXWormXXXXXXXXX
Huntington disease-like-4607136Graph: Huntington disease-like-4MouseHumanXWormXXXXXXYeastXPfalc
Hyalinosis, infantile systemic236490Graph: Hyalinosis, infantile systemicXHumanXXXXXXXXXXX
Hydrocephalus due to aqueductal stenosis307000Graph: Hydrocephalus due to aqueductal stenosisMouseHumanXXXXXZfinXXXXX
Hydrocephalus with Hirschsprung disease and cleft palate142623Graph: Hydrocephalus with Hirschsprung disease and cleft palateMouseHumanRatXXXXZfinXXXXX
Hydrocephalus with congenital idiopathic intestinal pseudoobstruction307000Graph: Hydrocephalus with congenital idiopathic intestinal pseudoobstructionMouseHumanXXXXXZfinXXXXX
Hyper-IgD syndrome260920Graph: Hyper-IgD syndromeMouseHumanXXXXXXXXYeastXX
Hyperalphalipoproteinemia143470Graph: HyperalphalipoproteinemiaXHumanXXXXXXXXXXX
Hyperbilirubinemia, familial transcient neonatal237900Graph: Hyperbilirubinemia, familial transcient neonatalXXRatXXDictyXXXXXXX
Hypercholanemia, familial607748Graph: Hypercholanemia, familialMouseHumanRatXXXXXXXXXX
Hypercholesterolemia, due to ligand-defective apo B144010Graph: Hypercholesterolemia, due to ligand-defective apo BMouseHumanXXXXXXXXXXX
Hypercholesterolemia, familial143890Graph: Hypercholesterolemia, familialMouseHumanRatXXXXXXXXXX
Hypercholesterolemia, familial, 3603776Graph: Hypercholesterolemia, familial, 3MouseXXXXXXXXXYeastXX
Hypercholesterolemia, familial, autosomal recessive603813Graph: Hypercholesterolemia, familial, autosomal recessiveXXXXXXXXXXXXX
Hypercholesterolemia, familial, modification of143890Graph: Hypercholesterolemia, familial, modification ofMouseHumanRatXXXXXXXXXX
Hypereosinophilic syndrome, idiopathic, resistant to imatinib607685Graph: Hypereosinophilic syndrome, idiopathic, resistant to imatinibMouseHumanRatXXXXXXXXXX
Hyperferritinemia-cataract syndrome600886Graph: Hyperferritinemia-cataract syndromeXHumanXXXXXXXXXXX
Hyperinsulinemic hypoglycemia, familial, 1256450Graph: Hyperinsulinemic hypoglycemia, familial, 1XHumanRatXXXXXXXXXX
Hyperinsulinemic hypoglycemia, familial, 2601820Graph: Hyperinsulinemic hypoglycemia, familial, 2XHumanXXXXXXXXXXX
Hyperinsulinemic hypoglycemia, familial, 3602485Graph: Hyperinsulinemic hypoglycemia, familial, 3MouseHumanRatXXXXXXXYeastXX
Hyperinsulinemic hypoglycemia, familial, 5609968Graph: Hyperinsulinemic hypoglycemia, familial, 5MouseHumanXWormXXChickenXXXXXX
Hyperinsulinism-hyperammonemia syndrome606762Graph: Hyperinsulinism-hyperammonemia syndromeMouseHumanXXXXXXXXYeastXPfalc
Hyperkalemic periodic paralysis170500Graph: Hyperkalemic periodic paralysisXHumanXXXXXXXXXXX
Hyperkeratotic cutaneous capillary-venous malformations associated with cerebral capillary malformations116860Graph: Hyperkeratotic cutaneous capillary-venous malformations associated with cerebral capillary malformationsXHumanXXXXXXXXXXX
Hyperlipoproteinemia, type Ib207750Graph: Hyperlipoproteinemia, type IbXXXXXXXXXXXXX
Hyperlysinemia238700Graph: HyperlysinemiaMouseHumanXXXXXXXXYeastXX
Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome238970Graph: Hyperornithinemia-hyperammonemia-homocitrullinemia syndromeMouseHumanXXXXXXXXXXX
Hyperostosis, endosteal144750Graph: Hyperostosis, endostealMouseHumanXXXDictyXXXXXXX
Hyperoxaluria, primary, type 1259900Graph: Hyperoxaluria, primary, type 1XHumanXXXXXXXXYeastXX
Hyperoxaluria, primary, type II260000Graph: Hyperoxaluria, primary, type IIXHumanXXXXXXXXXXX
Hyperparathyroidism, AD145000Graph: Hyperparathyroidism, ADMouseHumanXXXXXXXXXXX
Hyperparathyroidism, familial primary145000Graph: Hyperparathyroidism, familial primaryMouseHumanXXXXXXXXXXX
Hyperparathyroidism, neonatal239200Graph: Hyperparathyroidism, neonatalXHumanRatXXXXXXXXXX
Hyperparathyroidism-jaw tumor syndrome145001Graph: Hyperparathyroidism-jaw tumor syndromeXXXXXXXXXXXXX
Hyperphenylalaninemia due to pterin-4a-carbinolamine dehydratase deficiency264070Graph: Hyperphenylalaninemia due to pterin-4a-carbinolamine dehydratase deficiencyXXXXXXXXXXXXX
Hyperprolinemia, type I239500Graph: Hyperprolinemia, type IMouseHumanXXXXXXXXYeastXX
Hyperprolinemia, type II239510Graph: Hyperprolinemia, type IIMouseHumanXWormXXXXXXYeastXX
Hypertension, early-onset, autosomal dominant, with exacerbation in pregnancy605115Graph: Hypertension, early-onset, autosomal dominant, with exacerbation in pregnancyMouseHumanXXXXXXXXXXX
Hypertension, essential145500Graph: Hypertension, essentialXHumanRatXXXXXXXXXX
Hyperthroidism, familial gestational603373Graph: Hyperthroidism, familial gestationalMouseHumanRatXXXXXXXXXX
Hyperthyroidism, nonautoimmune609152Graph: Hyperthyroidism, nonautoimmuneMouseHumanRatXXXXXXXXXX
Hyperuricemic nephropathy, familial juvenile162000Graph: Hyperuricemic nephropathy, familial juvenileXHumanRatXXXXXXXXXX
Hypoaldosteronism, congenital, due to CMO I deficiency203400Graph: Hypoaldosteronism, congenital, due to CMO I deficiencyXHumanRatXXXXXXXXXX
Hypocalcemia, autosomal dominant146200Graph: Hypocalcemia, autosomal dominantXHumanRatXXXXXXXXXX
Hypocalciuric hypercalcemia, type I145980Graph: Hypocalciuric hypercalcemia, type IXHumanRatXXXXXXXXXX
Hypochondroplasia146000Graph: HypochondroplasiaMouseHumanXWormXXXXXXXXX
Hypodontia106600Graph: HypodontiaMouseHumanXWormXXXXXXXXX
Hypodontia with orofacial cleft106600Graph: Hypodontia with orofacial cleftMouseHumanXWormXXXXXXXXX
Hypodontia, autosomal dominant106600Graph: Hypodontia, autosomal dominantMouseHumanXWormXXXXXXXXX
Hypoglycemia of infancy, leucine-sensitive240800Graph: Hypoglycemia of infancy, leucine-sensitiveXHumanRatXXXXXXXXXX
Hypogonadotropic hypogonadism146110Graph: Hypogonadotropic hypogonadismMouseHumanXXXXXXXXXXX
Hypogonadotropic hypogonadism due to GNRH deficiency227200Graph: Hypogonadotropic hypogonadism due to GNRH deficiencyXHumanRatXXXChickenXXXXXX
Hypokalemic periodic paralysis170400Graph: Hypokalemic periodic paralysisXHumanRatWormXXXXXXXXX
Hypolactasia, adult type223100Graph: Hypolactasia, adult typeXHumanXXXXXXXXXXX
Hypomagnesemia with secondary hypocalcemia602014Graph: Hypomagnesemia with secondary hypocalcemiaXXXWormXXXXXXXXX
Hypomagnesemia, primary248250Graph: Hypomagnesemia, primaryXHumanRatXXXXXXXXXX
Hypomagnesemia-2, renal154020Graph: Hypomagnesemia-2, renalXHumanXXXXXXXXXXX
Hypoparathyroidism, sensorineural deafness, and renal dysplasia146255Graph: Hypoparathyroidism, sensorineural deafness, and renal dysplasiaMouseHumanXWormXXXXXXXXX
Hypoparathyroidism-retardation-dysmorphism syndrome241410Graph: Hypoparathyroidism-retardation-dysmorphism syndromeMouseHumanXXXXXXXXYeastXX
Hypophosphatasia, childhood241510Graph: Hypophosphatasia, childhoodXXRatXXXXXXXYeastXX
Hypophosphatasia, infantile241500Graph: Hypophosphatasia, infantileXXRatXXXXXXXYeastXX
Hypophosphatemic rickets, autosomal dominant193100Graph: Hypophosphatemic rickets, autosomal dominantMouseXXXXXXXXXXXX
Hypoplastic enamel pitting, localized608563Graph: Hypoplastic enamel pitting, localizedXXXXXXXXXXXXX
Hypoplastic left heart syndrome241550Graph: Hypoplastic left heart syndromeMouseHumanRatXXXXZfinXXXXX
Hypothyroidism, congenital274400Graph: Hypothyroidism, congenitalMouseHumanRatXXXXXXXYeastXX
Hypothyroidism, congenital, due to DUOX2 deficiency607200Graph: Hypothyroidism, congenital, due to DUOX2 deficiencyXHumanXWormXXXXXXYeastXX
Hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia218700Graph: Hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasiaMouseHumanRatXXXXXXXXXX
Hypotrichosis simplex of scalp146520Graph: Hypotrichosis simplex of scalpMouseHumanXXXXXXXXXXX
Hypotrichosis, congential, with juvenile macular dystrophy601553Graph: Hypotrichosis, congential, with juvenile macular dystrophyMouseHumanXXXXXXXXXXX
Hypotrichosis, localized, autosomal recessive607903Graph: Hypotrichosis, localized, autosomal recessiveMouseXRatXXXXXXXXXX
Hypotrichosis-lymphedema-telangiectasia syndrome607823Graph: Hypotrichosis-lymphedema-telangiectasia syndromeXXXXXXXXXXXXX
Hypouricemia, renal220150Graph: Hypouricemia, renalXXXXXXXXXXXXX
Hystrix-like ichthyosis with deafness602540Graph: Hystrix-like ichthyosis with deafnessMouseHumanRatXXXXXXXXXX

I
OMIM disorder(s)OMIM_idComparisonGraphMouseHumanRatWormFlyDictyChickenZfinRiceTairYeastPombePfalc
ICOS deficiency607594Graph: ICOS deficiencyXXXXXXXXXXXXX
IRAK4 deficiency607676Graph: IRAK4 deficiencyMouseHumanXXXXXZfinXXXXX
Ichthyosiform erythroderma, congenital242100Graph: Ichthyosiform erythroderma, congenitalMouseHumanXXXDictyXXRiceXXXX
Ichthyosiform erythroderma, congenital, nonbullous, 1242100Graph: Ichthyosiform erythroderma, congenital, nonbullous, 1MouseHumanXXXDictyXXRiceXXXX
Ichthyosis bullosa of Siemens146800Graph: Ichthyosis bullosa of SiemensXHumanXXXXXXXXXXX
Ichthyosis histrix, Curth-Macklin type146590Graph: Ichthyosis histrix, Curth-Macklin typeXHumanXXXXXXXXXXX
Ichthyosis vulgaris146700Graph: Ichthyosis vulgarisXHumanXXXXXXXXXXX
Ichthyosis, cyclic, with epidermolytic hyperkeratosis607602Graph: Ichthyosis, cyclic, with epidermolytic hyperkeratosisMouseHumanXXXXXXXXXXX
Ichthyosis, harlequin242500Graph: Ichthyosis, harlequinXXXXXXXXXXXXX
Ichthyosis, lamellar 2601277Graph: Ichthyosis, lamellar 2XXXXXXXXXXXXX
Ichthyosis, lamellar, autosomal recessive242300Graph: Ichthyosis, lamellar, autosomal recessiveMouseHumanXXXXXXXXXXX
Immunodeficiency due to defect in CD3-zeta610163Graph: Immunodeficiency due to defect in CD3-zetaXHumanXXXXXXXXXXX
Immunodeficiency with hyper IgM, type 4608106Graph: Immunodeficiency with hyper IgM, type 4MouseHumanXXXXXXXXYeastXX
Immunodeficiency with hyper-IgM, type 2605258Graph: Immunodeficiency with hyper-IgM, type 2MouseXXXXXXXXXXXX
Immunodeficiency with hyper-IgM, type 3606843Graph: Immunodeficiency with hyper-IgM, type 3XHumanXXXXXXXXXXX
Immunodeficiency, X-linked, with hyper-IgM308230Graph: Immunodeficiency, X-linked, with hyper-IgMXHumanXXXXXXXXXXX
Immunodeficiency, isolated300584Graph: Immunodeficiency, isolatedMouseHumanRatXXXXXXXXXX
Immunodeficiency-centromeric instability-facial anomalies syndrome242860Graph: Immunodeficiency-centromeric instability-facial anomalies syndromeMouseHumanXXXXXXXXXXX
Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked304790Graph: Immunodysregulation, polyendocrinopathy, and enteropathy, X-linkedMouseHumanXXXXXXXXXXX
Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia167320Graph: Inclusion body myopathy with early-onset Paget disease and frontotemporal dementiaMouseHumanXXXXXXXXYeastXX
Inclusion body myopathy, autosomal recessive600737Graph: Inclusion body myopathy, autosomal recessiveMouseHumanRatXXXXXXXXXX
Inclusion body myopathy-3605637Graph: Inclusion body myopathy-3XHumanXWormXDictyXXXXYeastPombeX
Incontinentia pigmenti, type II308300Graph: Incontinentia pigmenti, type IIMouseHumanRatXXXXXXXXXX
Infantile spasm syndrome308350Graph: Infantile spasm syndromeMouseXXXXXXXXXYeastXX
Insensitivity to pain, congenital, with anhidrosis256800Graph: Insensitivity to pain, congenital, with anhidrosisXHumanXXXXXXXXXXX
Insomnia, fatal familial600072Graph: Insomnia, fatal familialMouseHumanRatXXXXXXXXXX
Insulin resistance, severe, digenic604367Graph: Insulin resistance, severe, digenicMouseHumanRatXXXXXXXXXX
Iridogoniodysgenesis601631Graph: IridogoniodysgenesisMouseHumanRatXXXXXXXXXX
Iridogoniodysgenesis syndrome-2137600Graph: Iridogoniodysgenesis syndrome-2MouseHumanXXXXXXXXYeastXX
Isovaleric acidemia243500Graph: Isovaleric acidemiaMouseHumanRatXXXXXXXXXX

J
OMIM disorder(s)OMIM_idComparisonGraphMouseHumanRatWormFlyDictyChickenZfinRiceTairYeastPombePfalc
Jackson-Weiss syndrome123150Graph: Jackson-Weiss syndromeMouseHumanRatWormXXXXXXXXX
Jensen syndrome311150Graph: Jensen syndromeMouseHumanRatXXXXXXXYeastXX
Jervell and Lange-Nielsen syndrome220400Graph: Jervell and Lange-Nielsen syndromeMouseHumanRatXXXXXXXXXX
Joubert syndrome609583Graph: Joubert syndromeXHumanXXXXXXXXXXX
Joubert syndrome-3608629Graph: Joubert syndrome-3MouseXXXXXXXXXXXX
Juberg-Marsidi syndrome309590Graph: Juberg-Marsidi syndromeMouseHumanRatWormXXXXXXXXX
Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome175050Graph: Juvenile polyposis/hereditary hemorrhagic telangiectasia syndromeMouseHumanXXXXXXXXXXX

K
OMIM disorder(s)OMIM_idComparisonGraphMouseHumanRatWormFlyDictyChickenZfinRiceTairYeastPombePfalc
Kallmann syndrome 2147950Graph: Kallmann syndrome 2MouseHumanRatWormXXXXXXXXX
Kanzaki disease609242Graph: Kanzaki diseaseXHumanXXXXXXXXXXX
Kartagener syndrome244400Graph: Kartagener syndromeMouseHumanXXXXXXXXXXX
Kenny-Caffey syndrome-1244460Graph: Kenny-Caffey syndrome-1MouseHumanXXXXXXXXYeastXX
Keratitis148190Graph: KeratitisMouseHumanRatWormXXChickenXXXYeastXX
Keratitis-ichthyosis-deafness syndrome148210Graph: Keratitis-ichthyosis-deafness syndromeMouseHumanRatXXXXXXXXXX
Keratoconus148300Graph: KeratoconusMouseHumanXWormXXXXXXYeastXX
Keratoderma, palmoplantar, with deafness148350Graph: Keratoderma, palmoplantar, with deafnessMouseHumanRatXXXXXXXXXX
Keratosis follicularis spinulosa decalvans308800Graph: Keratosis follicularis spinulosa decalvansMouseHumanXXXXXXXXXXX
Keratosis palmoplantaria striata148700Graph: Keratosis palmoplantaria striataMouseHumanXXXXXXXXXXX
Keratosis palmoplantaris striata I148700Graph: Keratosis palmoplantaris striata IMouseHumanXXXXXXXXXXX
Keratosis palmoplantaris striata III607654Graph: Keratosis palmoplantaris striata IIIXHumanXXXXXXXXXXX
Keutel syndrome245150Graph: Keutel syndromeXHumanXXXXXXXXXXX
Kindler syndrome173650Graph: Kindler syndromeXXXWormXXXXXXXXX
Klippel-Trenaunay syndrome149000Graph: Klippel-Trenaunay syndromeXXXXXXXXXXXXX
Kniest dysplasia156550Graph: Kniest dysplasiaMouseHumanRatXXXXXXXXXX
Knobloch syndrome267750Graph: Knobloch syndromeMouseHumanXXXXXXXXXXX
Krabbe disease245200Graph: Krabbe diseaseMouseHumanXXXXXXXXXXX

L
OMIM disorder(s)OMIM_idComparisonGraphMouseHumanRatWormFlyDictyChickenZfinRiceTairYeastPombePfalc
LADD syndrome149730Graph: LADD syndromeMouseHumanXWormXXXXXXXXX
LIG4 syndrome606593Graph: LIG4 syndromeMouseHumanXXXXXXXXYeastXX
Lacticacidemia due to PDX1 deficiency245349Graph: Lacticacidemia due to PDX1 deficiencyMouseXXXXXXXXXXXX
Lactoferrin-deficient neutrophils245480Graph: Lactoferrin-deficient neutrophilsXHumanXXXXXXXXXXX
Langer mesomelic dysplasia249700Graph: Langer mesomelic dysplasiaXXXXXXXXXXXXX
Laron dwarfism262500Graph: Laron dwarfismMouseHumanRatXXXXXXXXXX
Larson syndrome150250Graph: Larson syndromeMouseHumanXXXDictyXXXXXXX
Laryngoonychocutaneous syndrome245660Graph: Laryngoonychocutaneous syndromeMouseHumanRatXXXXXXXXXX
Lathosterolosis607330Graph: LathosterolosisXHumanXXXXXXXXYeastXX
Leber congenital amaurosis204000Graph: Leber congenital amaurosisMouseHumanRatXXXXXXXXXX
Leber congenital amaurosis, type I204000Graph: Leber congenital amaurosis, type IMouseHumanRatXXXXXXXXXX
Leber congenital amaurosis, type III604232Graph: Leber congenital amaurosis, type IIIXHumanXXXXXXXXXXX
Leber congenital amaurosis-2204100Graph: Leber congenital amaurosis-2MouseHumanXXXXXXXXXXX
Left ventricular noncompaction with congenital heart defects606617Graph: Left ventricular noncompaction with congenital heart defectsMouseHumanXXXXXXXXXXX
Left ventricular noncompaction, familial isolated, 1604169Graph: Left ventricular noncompaction, familial isolated, 1MouseHumanXXXXXXXXXXX
Leigh syndrome256000Graph: Leigh syndromeMouseHumanXWormXXXXXXYeastXX
Leigh syndrome due to cytochrome c oxidase deficiency256000Graph: Leigh syndrome due to cytochrome c oxidase deficiencyMouseHumanXWormXXXXXXYeastXX
Leigh syndrome, French-Canadian type220111Graph: Leigh syndrome, French-Canadian typeMouseHumanXXXXXXXXXXX
Leigh syndrome, due to COX deficiency256000Graph: Leigh syndrome, due to COX deficiencyMouseHumanXWormXXXXXXYeastXX
Leiomyomatosis and renal cell cancer605839Graph: Leiomyomatosis and renal cell cancerMouseHumanXWormXXXXXXYeastXX
Leiomyomatosis, diffuse, with Alport syndrome308940Graph: Leiomyomatosis, diffuse, with Alport syndromeMouseXXXXXXXXXXXX
Leopard syndrome151100Graph: Leopard syndromeMouseHumanXWormXXXXXXXXX
Leprechaunism246200Graph: LeprechaunismMouseHumanXWormXXChickenXXXXXX
Leri-Weill dyschondrosteosis127300Graph: Leri-Weill dyschondrosteosisXXXXXXXXXXXXX
Leukemia, acute myelogenous601626Graph: Leukemia, acute myelogenousMouseHumanRatWormXXXXXXYeastXX
Leukemia, acute myeloid601626Graph: Leukemia, acute myeloidMouseHumanRatWormXXXXXXYeastXX
Leukemia, acute myeloid, somatic601626Graph: Leukemia, acute myeloid, somaticMouseHumanRatWormXXXXXXYeastXX
Leukemia, chronic myeloid608232Graph: Leukemia, chronic myeloidMouseHumanXXXXXXXXXXX
Leukemia, juvenile myelomonocytic607785Graph: Leukemia, juvenile myelomonocyticMouseHumanXWormXXXXXXXXX
Leukemia, megakaryoblastic, of Down syndrome190685Graph: Leukemia, megakaryoblastic, of Down syndromeMouseHumanRatXXXXXXXXXX
Leukemia, megakaryoblastic, with or without Down syndrome190685Graph: Leukemia, megakaryoblastic, with or without Down syndromeMouseHumanRatXXXXXXXXXX
Leukemia/lymphoma, chronic B-cell151400Graph: Leukemia/lymphoma, chronic B-cellMouseHumanRatWormXXXXXXXXX
Leukocyte adhesion deficiency116920Graph: Leukocyte adhesion deficiencyMouseHumanXWormXXXXXXXXX
Leukoencephalopathy with vanishing white matter603896Graph: Leukoencephalopathy with vanishing white matterMouseHumanRatWormXXXXXXYeastXX
Leukoencephaly with vanishing white matter603896Graph: Leukoencephaly with vanishing white matterMouseHumanRatWormXXXXXXYeastXX
Li Fraumeni syndrome151623Graph: Li Fraumeni syndromeMouseHumanRatXXXXXXXXXX
Li-Fraumeni syndrome151623Graph: Li-Fraumeni syndromeMouseHumanRatXXXXXXXXXX
Liddle syndrome177200Graph: Liddle syndromeMouseHumanXWormXXXXXXXXX
Limb-mammary syndrome603543Graph: Limb-mammary syndromeMouseHumanRatXXXXXXXXXX
Lipodystrophy, congenital generalized, type 1608594Graph: Lipodystrophy, congenital generalized, type 1XHumanXXXXXXXXYeastXX
Lipodystrophy, congenital generalized, type 2269700Graph: Lipodystrophy, congenital generalized, type 2XHumanXXXXXXXXXXX
Lipodystrophy, familial partial151660Graph: Lipodystrophy, familial partialMouseHumanRatWormXXXXXXXXX
Lipoid adrenal hyperplasia201710Graph: Lipoid adrenal hyperplasiaMouseXRatXXXXXXXXXX
Lipoid congenital adrenal hyperplasia201710Graph: Lipoid congenital adrenal hyperplasiaMouseXRatXXXXXXXXXX
Lipoid proteinosis247100Graph: Lipoid proteinosisMouseHumanXXXXXXXXXXX
Lipomatosis, mutiple151900Graph: Lipomatosis, mutipleMouseHumanXXXXXXXXXXX
Lissencephaly, X-linked300067Graph: Lissencephaly, X-linkedMouseHumanXWormXXXXXXXXX
Lissencephaly, X-linked with ambiguous genitalia300215Graph: Lissencephaly, X-linked with ambiguous genitaliaMouseXXXXXXXXXYeastXX
Lissencephaly-1607432Graph: Lissencephaly-1MouseHumanRatWormXDictyXXXXXXX
Loeys-Dietz syndrome609192Graph: Loeys-Dietz syndromeMouseHumanRatXXXXXXXXXX
Long QT syndrome-1192500Graph: Long QT syndrome-1MouseHumanRatXXXXXXXXXX
Long QT syndrome-3603830Graph: Long QT syndrome-3XHumanRatXXXXXXXXXX
Long QT syndrome-4600919Graph: Long QT syndrome-4XXRatWormXXXXXXXXX
Long QT syndrome-7170390Graph: Long QT syndrome-7XHumanXXXXXXXXXXX
Lower motor neuron disease, progressive, without sensory symptoms607641Graph: Lower motor neuron disease, progressive, without sensory symptomsMouseXRatWormXXXXXXXXX
Lung cancer211980Graph: Lung cancerMouseHumanRatWormXDictyXXXXYeastXX
Lymphangioleiomyomatosis606690Graph: LymphangioleiomyomatosisMouseHumanRatXXXXXXXXXX
Lymphangioleiomyomatosis, somatic606690Graph: Lymphangioleiomyomatosis, somaticMouseHumanRatXXXXXXXXXX
Lymphedema and ptosis153000Graph: Lymphedema and ptosisMouseHumanRatXXXXXXXXXX
Lymphedema, hereditary I153100Graph: Lymphedema, hereditary IMouseHumanRatWormXXXXXXXXX
Lymphedema, hereditary II153200Graph: Lymphedema, hereditary IIMouseHumanRatXXXXXXXXXX
Lymphedema-distichiasis syndrome153400Graph: Lymphedema-distichiasis syndromeMouseHumanRatXXXXXXXXXX
Lymphoma, non-Hodgkin605027Graph: Lymphoma, non-HodgkinMouseHumanRatXXXXXXXXXX
Lymphoproliferative syndrome, X-linked308240Graph: Lymphoproliferative syndrome, X-linkedMouseHumanXXXXXXXXXXX
Lysinuric protein intolerance222700Graph: Lysinuric protein intoleranceXHumanXXXXXXXXYeastXX

M
OMIM disorder(s)OMIM_idComparisonGraphMouseHumanRatWormFlyDictyChickenZfinRiceTairYeastPombePfalc
MASA syndrome303350Graph: MASA syndromeMouseHumanXXXXXZfinXXXXX
MASS syndrome604308Graph: MASS syndromeMouseHumanXWormXXXXXXXXX
MHC class II deficiency, complementation group B209920Graph: MHC class II deficiency, complementation group BMouseHumanRatXXXXXXXXXX
MODY, one form125850Graph: MODY, one formMouseHumanRatXXXChickenXXXXXX
MODY, type I125850Graph: MODY, type IMouseHumanRatXXXChickenXXXXXX
MODY, type II125851Graph: MODY, type IIMouseHumanRatXXXXXXXYeastXX
MODY, type III600496Graph: MODY, type IIIMouseHumanRatXXXXXXXXXX
Machado-Joseph disease109150Graph: Machado-Joseph diseaseXHumanXXXXXXXXXXX
Macrocytic anemia, refractory, of 5q- syndrome153550Graph: Macrocytic anemia, refractory, of 5q- syndromeMouseHumanRatXXXXXXXXXX
Macrothrombocytopenia300367Graph: MacrothrombocytopeniaMouseHumanRatXXXXXXXXXX
Macrothrombocytopenia and progressive sensorineural deafness600208Graph: Macrothrombocytopenia and progressive sensorineural deafnessMouseXXWormXDictyXXXXYeastPombeX
Macular corneal dystrophy217800Graph: Macular corneal dystrophyXHumanXXXXXXXXXXX
Macular degeneration, age-related, 2153800Graph: Macular degeneration, age-related, 2MouseHumanXXXXXXXXXXX
Macular degeneration, age-related, 3608895Graph: Macular degeneration, age-related, 3XHumanRatXXXXXXXXXX
Macular degeneration, juvenile248200Graph: Macular degeneration, juvenileMouseHumanXXXXXXXXXXX
Macular dystrophy, autosomal dominant, chromosome 6-linked600110Graph: Macular dystrophy, autosomal dominant, chromosome 6-linkedXXXXXXXXXXYeastXX
Macular dystrophy, vitelliform608161Graph: Macular dystrophy, vitelliformXHumanXXXXXXXXXXX
Macular dystrophy, vitelliform type153700Graph: Macular dystrophy, vitelliform typeXHumanXXXXXXXXXXX
Maculopathy, bull's-eye153870Graph: Maculopathy, bull's-eyeXHumanXXXXXXXXXXX
Malonyl-CoA decarboxylase deficiency248360Graph: Malonyl-CoA decarboxylase deficiencyXHumanRatXXXXXXXXXX
Mandibuloacral dysplasia with type B lipodystrophy608612Graph: Mandibuloacral dysplasia with type B lipodystrophyMouseHumanXXXXXXXXYeastXX
Maple syrup urine disease, type Ia248600Graph: Maple syrup urine disease, type IaMouseHumanRatXXDictyXXXXXXX
Marfan syndrome154700Graph: Marfan syndromeMouseHumanXWormXXXXXXXXX
Marshall syndrome154780Graph: Marshall syndromeMouseHumanXXXXXXXXXXX
Mast syndrome248900Graph: Mast syndromeXXXXXXXXXXXXX
May-Hegglin anomaly155100Graph: May-Hegglin anomalyMouseXXWormXDictyXXXXYeastPombeX
McArdle disease232600Graph: McArdle diseaseMouseHumanRatXXDictyXXXXYeastXX
McCune-Albright syndrome174800Graph: McCune-Albright syndromeMouseXRatWormXXXXXXXXX
McKusick-Kaufman syndrome236700Graph: McKusick-Kaufman syndromeMouseHumanXXXXXXXXXXX
Medullary cystic kidney disease 2603860Graph: Medullary cystic kidney disease 2XHumanRatXXXXXXXXXX
Medullary thyroid carcinoma155240Graph: Medullary thyroid carcinomaMouseHumanXXXXXXXXXXX
Medullary thyroid carcinoma, familial155240Graph: Medullary thyroid carcinoma, familialMouseHumanXXXXXXXXXXX
Medulloblastoma155255Graph: MedulloblastomaMouseHumanRatWormXXXXXXXXX
Medulloblastoma, desmoplastic155255Graph: Medulloblastoma, desmoplasticMouseHumanRatWormXXXXXXXXX
Medulloblastoma, somatic155255Graph: Medulloblastoma, somaticMouseHumanRatWormXXXXXXXXX
Meesmann corneal dystrophy122100Graph: Meesmann corneal dystrophyXHumanXXXXXXXXXXX
Megacystis-microcolon-intestinal hypoperistalsis syndrome249210Graph: Megacystis-microcolon-intestinal hypoperistalsis syndromeXHumanRatWormXXXXXXXXX
Megalencephalic leukoencephalopathy with subcortical cysts604004Graph: Megalencephalic leukoencephalopathy with subcortical cystsXHumanXXXXXXXXXXX
Megaloblastic anemia-1, Finnish type261100Graph: Megaloblastic anemia-1, Finnish typeMouseHumanRatXXXXXXXXXX
Megaloblastic anemia-1, Norwegian type261100Graph: Megaloblastic anemia-1, Norwegian typeMouseHumanRatXXXXXXXXXX
Melanoma and neural system tumor syndrome155755Graph: Melanoma and neural system tumor syndromeXHumanXXXXXXXXXXX
Melanoma, cutaneous malignant, 2155601Graph: Melanoma, cutaneous malignant, 2XHumanXXXXXXXXXXX
Meleda disease248300Graph: Meleda diseaseXHumanXXXXXXXXXXX
Melnick-Needles syndrome309350Graph: Melnick-Needles syndromeMouseHumanXXXDictyXXXXXXX
Meningioma607174Graph: MeningiomaMouseHumanRatWormXDictyXXXXXXX
Meningioma, NF2-related, somatic607174Graph: Meningioma, NF2-related, somaticMouseHumanRatWormXDictyXXXXXXX
Menkes disease309400Graph: Menkes diseaseMouseHumanXWormXXXXXXYeastXX
Mental retardation in cri-du-chat syndrome123450Graph: Mental retardation in cri-du-chat syndromeXHumanXXXXXXXXXXX
Mental retardation, X-linked300495Graph: Mental retardation, X-linkedXXXXXXXXXXXXX
Mental retardation, X-linked 30300558Graph: Mental retardation, X-linked 30XXRatXXDictyXXXXYeastXX
Mental retardation, X-linked 36/43/54300419Graph: Mental retardation, X-linked 36/43/54MouseXXXXXXXXXYeastXX
Mental retardation, X-linked 45300498Graph: Mental retardation, X-linked 45XXXXXXXXXTairYeastXX
Mental retardation, X-linked 58300218Graph: Mental retardation, X-linked 58XXXXXXXXXXXXX
Mental retardation, X-linked nonspecific309541Graph: Mental retardation, X-linked nonspecificXHumanRatWormXXXXXXYeastXX
Mental retardation, X-linked nonspecific, 63300387Graph: Mental retardation, X-linked nonspecific, 63MouseXRatXXXXXXXYeastXX
Mental retardation, X-linked nonspecific, type 46300436Graph: Mental retardation, X-linked nonspecific, type 46XHumanXXXXXXXXXXX
Mental retardation, X-linked, 21/34300143Graph: Mental retardation, X-linked, 21/34XXXXXXXXXXXXX
Mental retardation, X-linked, Snyder-Robinson type309583Graph: Mental retardation, X-linked, Snyder-Robinson typeMouseHumanXXXXXXXXXXX
Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance300486Graph: Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearanceMouseHumanXXXXXXXXXXX
Mental retardation, X-linked, with isolated growth hormone deficiency300123Graph: Mental retardation, X-linked, with isolated growth hormone deficiencyMouseHumanXXXXXXXXXXX
Mental retardation, X-linked, with progressive spasticity300279Graph: Mental retardation, X-linked, with progressive spasticityXHumanXXXXXXXXXXX
Mental retardation, X-linked-44300501Graph: Mental retardation, X-linked-44XXXXXXXXXXYeastXX
Mental retardation, X-linked-9309549Graph: Mental retardation, X-linked-9XXXXXXXXXXYeastXX
Mental retardation, autosomal recessive 1249500Graph: Mental retardation, autosomal recessive 1XXXXXXXXXXXXX
Mesangial sclerosis, isolated diffuse256370Graph: Mesangial sclerosis, isolated diffuseMouseXXXXXXXXXXXX
Metachromatic leukodystrophy250100Graph: Metachromatic leukodystrophyMouseHumanXXXXXXXXXXX
Metaphyseal chondrodysplasia, Murk Jansen type156400Graph: Metaphyseal chondrodysplasia, Murk Jansen typeMouseHumanRatXXXXXXXXXX
Methylcobalamin deficiency, cblG type250940Graph: Methylcobalamin deficiency, cblG typeMouseXRatXXXXXXXYeastXX
Methylmalonic aciduria, vitamin B12-responsive251100Graph: Methylmalonic aciduria, vitamin B12-responsiveXXXXXXXXXXXXX
Methylmalonic aciduria, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin, cblB complementation type251110Graph: Methylmalonic aciduria, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin, cblB complementation typeXXXXXXXXXXXXX
Microcephaly, Amish type607196Graph: Microcephaly, Amish typeXHumanXXXXXXXXYeastXX
Microcephaly, autosomal recessive 1251200Graph: Microcephaly, autosomal recessive 1XXXXXXXXXXXXX
Microcephaly, primary autosomal recessive, 5608716Graph: Microcephaly, primary autosomal recessive, 5XXXXXXXXXXXXX
Microphthalmia with associated anomalies 2300412Graph: Microphthalmia with associated anomalies 2XHumanXXXXXXXXXXX
Migraine, familial basilar602481Graph: Migraine, familial basilarMouseXRatWormXXXZfinXXXXX
Migraine, familial hemiplegic, 2602481Graph: Migraine, familial hemiplegic, 2MouseXRatWormXXXZfinXXXXX
Migraine, familial hemiplegic, 3609634Graph: Migraine, familial hemiplegic, 3XXRatXXXXXXXXXX
Miller-Dieker lissencephaly247200Graph: Miller-Dieker lissencephalyMouseXRatXXDictyXXRiceXYeastXX
Mirror-image polydactyly135750Graph: Mirror-image polydactylyXXXXXXXXXXXXX
Mitochondrial DNA-depletion syndrome, hepatocerebral form251880Graph: Mitochondrial DNA-depletion syndrome, hepatocerebral formMouseHumanXXXXXXXXXXX
Mitochondrial complex I deficiency252010Graph: Mitochondrial complex I deficiencyMouseHumanXWormXXXXXXXXX
Mitochondrial complex III deficiency124000Graph: Mitochondrial complex III deficiencyMouseHumanXXXXXXXXYeastXX
Mitochondrial neurogastrointestinal encephalomyopathy syndrome603041Graph: Mitochondrial neurogastrointestinal encephalomyopathy syndromeMouseHumanXXXXXXXXXXX
Mitochondrial respiratory chain complex II deficiency252011Graph: Mitochondrial respiratory chain complex II deficiencyMouseHumanXXXXXXXXYeastXX
Miyoshi myopathy254130Graph: Miyoshi myopathyMouseHumanXWormXXXXXXXXX
Mohr-Tranebjaerg syndrome304700Graph: Mohr-Tranebjaerg syndromeMouseHumanRatXXXXXXXYeastXX
Molybdenum cofactor deficiency, type A252150Graph: Molybdenum cofactor deficiency, type AMouseHumanRatXXXXXXXXXX
Molybdenum cofactor deficiency, type B252150Graph: Molybdenum cofactor deficiency, type BMouseHumanRatXXXXXXXXXX
Molybdenum cofactor deficiency, type C252150Graph: Molybdenum cofactor deficiency, type CMouseHumanRatXXXXXXXXXX
Monilethrix158000Graph: MonilethrixXHumanXXXXXXXXXXX
Mowat-Wilson syndrome235730Graph: Mowat-Wilson syndromeMouseHumanXWormXXXXXTairYeastXX
Muckle-Wells syndrome191900Graph: Muckle-Wells syndromeXHumanXXXDictyXXXXXXX
Mucolipidosis IIIC252605Graph: Mucolipidosis IIICXXXXXXXXXXXXX
Mucolipidosis IV252650Graph: Mucolipidosis IVXXXWormXXXXXXXXX
Mucopolysaccharidosis Ih607014Graph: Mucopolysaccharidosis IhXHumanXXXXXXXXXXX
Mucopolysaccharidosis Ih/s607015Graph: Mucopolysaccharidosis Ih/sXHumanXXXXXXXXXXX
Mucopolysaccharidosis Is607016Graph: Mucopolysaccharidosis IsXHumanXXXXXXXXXXX
Mucopolysaccharidosis type IIID252940Graph: Mucopolysaccharidosis type IIIDXHumanXXXXXXXXXXX
Mucopolysaccharidosis type IX601492Graph: Mucopolysaccharidosis type IXXHumanXXXXXXXXXXX
Muenke syndrome602849Graph: Muenke syndromeMouseHumanXWormXXXXXXXXX
Muir-Torre syndrome158320Graph: Muir-Torre syndromeMouseHumanXXXXXXXXYeastXX
Mulibrey nanism253250Graph: Mulibrey nanismXHumanXXXXXXXXXXX
Multiple cutaneous and uterine leiomyomata150800Graph: Multiple cutaneous and uterine leiomyomataMouseHumanXWormXXXXXXYeastXX
Multiple endocrine neoplasia IIA171400Graph: Multiple endocrine neoplasia IIAMouseHumanXXXXXXXXXXX
Multiple endocrine neoplasia IIB162300Graph: Multiple endocrine neoplasia IIBMouseHumanXXXXXXXXXXX
Multiple myeloma254500Graph: Multiple myelomaMouseHumanRatWormXXXXXXXXX
Multiple sulfatase deficiency272200Graph: Multiple sulfatase deficiencyXXXXXXXXXXXXX
Muscle glycogenosis300559Graph: Muscle glycogenosisXHumanRatXXXXXXXXXX
Muscle-eye-brain disease253280Graph: Muscle-eye-brain diseaseMouseXXXXXXXXXXXX
Muscular dystrophy with epidermolysis bullosa simplex226670Graph: Muscular dystrophy with epidermolysis bullosa simplexMouseHumanRatXXDictyXXXXXXX
Muscular dystrophy, Fukuyama congenital253800Graph: Muscular dystrophy, Fukuyama congenitalMouseHumanXXXXXXXXXXX
Muscular dystrophy, congenital merosin-deficient607855Graph: Muscular dystrophy, congenital merosin-deficientMouseHumanXWormXXXXXXXXX
Muscular dystrophy, congenital, 1C606612Graph: Muscular dystrophy, congenital, 1CMouseXXXXXXXXXXXX
Muscular dystrophy, congenital, due to partial LAMA2 deficiency607855Graph: Muscular dystrophy, congenital, due to partial LAMA2 deficiencyMouseHumanXWormXXXXXXXXX
Muscular dystrophy, congenital, type 1D608840Graph: Muscular dystrophy, congenital, type 1DXHumanXXXXXXXXXXX
Muscular dystrophy, limb-girdle, type 1A159000Graph: Muscular dystrophy, limb-girdle, type 1AXHumanXXXXXXXXXXX
Muscular dystrophy, limb-girdle, type 2A253600Graph: Muscular dystrophy, limb-girdle, type 2AXHumanXXXDictyXXXXYeastXX
Muscular dystrophy, limb-girdle, type 2B253601Graph: Muscular dystrophy, limb-girdle, type 2BMouseHumanXWormXXXXXXXXX
Muscular dystrophy, limb-girdle, type 2D608099Graph: Muscular dystrophy, limb-girdle, type 2DXHumanXXXXXXXXXXX
Muscular dystrophy, limb-girdle, type 2E604286Graph: Muscular dystrophy, limb-girdle, type 2EMouseHumanXXXXXXXXXXX
Muscular dystrophy, limb-girdle, type 2F601287Graph: Muscular dystrophy, limb-girdle, type 2FMouseHumanXXXXXXXXXXX
Muscular dystrophy, limb-girdle, type 2G601954Graph: Muscular dystrophy, limb-girdle, type 2GXHumanXXXXXXXXXXX
Muscular dystrophy, limb-girdle, type 2H254110Graph: Muscular dystrophy, limb-girdle, type 2HMouseHumanXXXXXXXXXXX
Muscular dystrophy, limb-girdle, type 2I607155Graph: Muscular dystrophy, limb-girdle, type 2IMouseXXXXXXXXXXXX
Muscular dystrophy, limb-girdle, type 2J608807Graph: Muscular dystrophy, limb-girdle, type 2JMouseHumanRatWormXXXXXXXXPfalc
Muscular dystrophy, limb-girdle, type 2K609308Graph: Muscular dystrophy, limb-girdle, type 2KMouseHumanXXXXXXXXXXX
Muscular dystrophy, limb-girdle, type IC607801Graph: Muscular dystrophy, limb-girdle, type ICMouseHumanRatWormXXXXXXXXX
Muscular dystrophy, rigid spine, 1602771Graph: Muscular dystrophy, rigid spine, 1XXXXXXXXXXXXX
Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency608931Graph: Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiencyMouseHumanRatXXXXXXXXXX
Myasthenic syndrome, congenital, associated with episodic apnea254210Graph: Myasthenic syndrome, congenital, associated with episodic apneaMouseHumanXXXXXXXXYeastXX
Myasthenic syndrome, congenital, associated with facial dysmorphism and acetylcholine receptor deficiency608931Graph: Myasthenic syndrome, congenital, associated with facial dysmorphism and acetylcholine receptor deficiencyMouseHumanRatXXXXXXXXXX
Myasthenic syndrome, fast-channel congenital608930Graph: Myasthenic syndrome, fast-channel congenitalMouseHumanRatXXXXZfinXXXXX
Myasthenic syndrome, slow-channel congenital601462Graph: Myasthenic syndrome, slow-channel congenitalMouseHumanRatXXXXZfinXXXXX
Mycobacterial infection, atypical, familial disseminated209950Graph: Mycobacterial infection, atypical, familial disseminatedMouseHumanRatXXXXXXXXXX
Myeloperoxidase deficiency254600Graph: Myeloperoxidase deficiencyMouseHumanXXXXXZfinXXXXX
Myeloproliferative disorder with eosinophilia131440Graph: Myeloproliferative disorder with eosinophiliaMouseHumanRatXXXXXXXXXX
Myoclonic epilepsy with mental retardation and spasticity300432Graph: Myoclonic epilepsy with mental retardation and spasticityMouseXXXXXXXXXYeastXX
Myoclonic epilepsy, juvenile, 1254770Graph: Myoclonic epilepsy, juvenile, 1MouseXXXXXXXXXXXX
Myoclonic epilepsy, severe, of infancy607208Graph: Myoclonic epilepsy, severe, of infancyMouseHumanRatXXXXXXXXXX
Myokymia with neonatal epilepsy606437Graph: Myokymia with neonatal epilepsyXHumanXXXXXXXXXXX
Myopathy due to CPT II deficiency255110Graph: Myopathy due to CPT II deficiencyMouseXRatXXXXXXXYeastXX
Myopathy, Laing distal160500Graph: Myopathy, Laing distalXHumanXWormXDictyXXXXYeastPombeX
Myopathy, actin, congenital, with excess of thin myofilaments161800Graph: Myopathy, actin, congenital, with excess of thin myofilamentsXHumanRatWormXXXXRiceXYeastXX
Myopathy, cardioskeletal, desmin-related, with cataract608810Graph: Myopathy, cardioskeletal, desmin-related, with cataractMouseHumanRatXXXXXXXXXX
Myopathy, centronuclear160150Graph: Myopathy, centronuclearMouseHumanXWormXXXXXXXXX
Myopathy, congenital, with fiber-type disporportion 1255310Graph: Myopathy, congenital, with fiber-type disporportion 1XHumanXXXXXXRiceXYeastXX
Myopathy, desmin-related, cardioskeletal601419Graph: Myopathy, desmin-related, cardioskeletalMouseHumanXXXXXXXXXXX
Myopathy, distal, with anterior tibial onset606768Graph: Myopathy, distal, with anterior tibial onsetMouseHumanXWormXXXXXXXXX
Myopathy, myosin storage608358Graph: Myopathy, myosin storageXHumanXWormXDictyXXXXYeastPombeX
Myopathy, nemaline, 3161800Graph: Myopathy, nemaline, 3XHumanRatWormXXXXRiceXYeastXX
Myopathy, proximal, with early respiratory muscle involvment603689Graph: Myopathy, proximal, with early respiratory muscle involvmentMouseHumanRatWormXXXXXXXXPfalc
Myopathy, spheroid body182920Graph: Myopathy, spheroid bodyXHumanXXXXXXXXXXX
Myotilinopathy609200Graph: MyotilinopathyXHumanXXXXXXXXXXX
Myotonia congenita, atypical, acetazolamide-responsive608390Graph: Myotonia congenita, atypical, acetazolamide-responsiveXHumanXXXXXXXXXXX
Myotonia congenita, dominant160800Graph: Myotonia congenita, dominantXHumanRatXXXXXXXXXX
Myotonia congenita, recessive255700Graph: Myotonia congenita, recessiveXHumanRatXXXXXXXXXX
Myotonic dystrophy160900Graph: Myotonic dystrophyXHumanXXXXXXXXXXX
Myotonic dystrophy, type 2602668Graph: Myotonic dystrophy, type 2MouseXRatXXXXXXXYeastXX
Myotubular myopathy, X-linked310400Graph: Myotubular myopathy, X-linkedMouseHumanXXXXXXXXXXX
Myxoma, intracardiac255960Graph: Myxoma, intracardiacMouseHumanRatWormXDictyXXXXXXX

N
OMIM disorder(s)OMIM_idComparisonGraphMouseHumanRatWormFlyDictyChickenZfinRiceTairYeastPombePfalc
N syndrome310465Graph: N syndromeXXRatXXXXXRiceXYeastXX
N-acetylglutamate synthase deficiency237310Graph: N-acetylglutamate synthase deficiencyMouseXXXXXXXXXYeastXX
Nail-patella syndrome161200Graph: Nail-patella syndromeMouseHumanXXXXXXXXXXX
Nail-patella syndrome with open-angle glaucoma137750Graph: Nail-patella syndrome with open-angle glaucomaMouseHumanRatXXXXXXXXXX
Nance-Horan syndrome302350Graph: Nance-Horan syndromeXXXXXXXXXXXXX
Narcolepsy161400Graph: NarcolepsyXHumanRatXXXXXXXXXX
Nasopharyngeal carcinoma161550Graph: Nasopharyngeal carcinomaMouseHumanRatXXXXXXXXXX
Nasu-Hakola disease221770Graph: Nasu-Hakola diseaseXHumanXXXXXXXXXXX
Naxos disease601214Graph: Naxos diseaseMouseHumanXWormXXXZfinXXXXX
Nemaline myopathy161800Graph: Nemaline myopathyXHumanRatWormXXXXRiceXYeastXX
Nemaline myopathy 1, autosomal dominant161800Graph: Nemaline myopathy 1, autosomal dominantXHumanRatWormXXXXRiceXYeastXX
Nemaline myopathy, Amish type605355Graph: Nemaline myopathy, Amish typeXHumanXWormXXXXXXYeastXX
Nephrolithiasis, type I310468Graph: Nephrolithiasis, type IMouseHumanRatXXXXXXXYeastXX
Nephronophthisis 2, infantile602088Graph: Nephronophthisis 2, infantileXXXXXXXZfinXXXXX
Nephronophthisis, juvenile256100Graph: Nephronophthisis, juvenileXHumanXXXXXXXXXXX
Nephrosis-1, congenital, Finnish type256300Graph: Nephrosis-1, congenital, Finnish typeMouseHumanXXXXXXXXXXX
Nephrotic syndrome, steroid-resistant600995Graph: Nephrotic syndrome, steroid-resistantMouseHumanXXXXXXXXXXX
Netherton syndrome256500Graph: Netherton syndromeMouseHumanXXXXXXXXXXX
Neuroblastoma256700Graph: NeuroblastomaMouseHumanRatXXDictyXXXXYeastXX
Neurodegeneration, pantothenate kinase-associated234200Graph: Neurodegeneration, pantothenate kinase-associatedXXXXXXXXXXXXX
Neuroectodermal tumors, supratentorial primitive, with cafe-au-lait spots608623Graph: Neuroectodermal tumors, supratentorial primitive, with cafe-au-lait spotsMouseHumanXWormXXXXXXYeastXX
Neurofibromatosis, familial spinal162210Graph: Neurofibromatosis, familial spinalMouseHumanXXXXXXXXXXX
Neurofibromatosis, type 2101000Graph: Neurofibromatosis, type 2MouseHumanXXXXXXXXXXX
Neurofibromatosis-Noonan syndrome601321Graph: Neurofibromatosis-Noonan syndromeMouseHumanXXXXXXXXXXX
Neuropathy, congenital hypomyelinating605253Graph: Neuropathy, congenital hypomyelinatingMouseHumanRatXXXXXXXYeastXX
Neuropathy, congenital hypomyelinating, 1605253Graph: Neuropathy, congenital hypomyelinating, 1MouseHumanRatXXXXXXXYeastXX
Neuropathy, distal hereditary motor608634Graph: Neuropathy, distal hereditary motorMouseHumanXXXXXXXXXXX
Neuropathy, distal hereditary motor, type II158590Graph: Neuropathy, distal hereditary motor, type IIMouseHumanXXXXXXXXXXX
Neuropathy, hereditary sensory and autonomic, type 1162400Graph: Neuropathy, hereditary sensory and autonomic, type 1XHumanXXXXXXXXYeastXX
Neuropathy, recurrent, with pressure palsies162500Graph: Neuropathy, recurrent, with pressure palsiesXHumanRatXXXXXXXXXX
Neutropenia, congenital202700Graph: Neutropenia, congenitalXHumanXXXXXXXXXXX
Neutropenia, severe congenital, X-linked300299Graph: Neutropenia, severe congenital, X-linkedMouseHumanXXXDictyXXXXYeastXX
Neutrophil immunodeficiency syndrome608203Graph: Neutrophil immunodeficiency syndromeMouseHumanXWormFlyDictyXXXTairXXX
Nevo syndrome601451Graph: Nevo syndromeXHumanXWormXXXXXXXXX
Nevus, epidermal, epidermolytic hyperkeratotic type600648Graph: Nevus, epidermal, epidermolytic hyperkeratotic typeMouseHumanXXXXXXXXXXX
Newfoundland rod-cone dystrophy607476Graph: Newfoundland rod-cone dystrophyMouseHumanXXXXXXXXXXX
Niemann-Pick disease, type A257200Graph: Niemann-Pick disease, type AXHumanXXXXXXXXYeastXX
Niemann-Pick disease, type B607616Graph: Niemann-Pick disease, type BXHumanXXXXXXXXYeastXX
Niemann-Pick disease, type C1257220Graph: Niemann-Pick disease, type C1MouseHumanXWormXXXXXXYeastXX
Niemann-Pick disease, type D257220Graph: Niemann-Pick disease, type DMouseHumanXWormXXXXXXYeastXX
Niemann-pick disease, type C2607625Graph: Niemann-pick disease, type C2XXXXXXXXXXXXX
Night blindness, congenital stationary, X-linked, type 2300071Graph: Night blindness, congenital stationary, X-linked, type 2XHumanRatWormXXXXXXXXX
Night blindness, congenital stationary, type 1310500Graph: Night blindness, congenital stationary, type 1MouseHumanXXXXXXXXXXX
Night blindness, congenital stationary, type 3163500Graph: Night blindness, congenital stationary, type 3MouseHumanXXXXXXXXXXX
Nijmegen breakage syndrome251260Graph: Nijmegen breakage syndromeMouseXRatXXXXXXXXXX
Non-Hodgkin lymphoma, somatic605027Graph: Non-Hodgkin lymphoma, somaticMouseHumanRatXXXXXXXXXX
Nonaka myopathy605820Graph: Nonaka myopathyMouseHumanRatXXXXXXXXXX
Noncompaction of left ventricular myocardium, isolated300183Graph: Noncompaction of left ventricular myocardium, isolatedXHumanXXXXXXXXYeastXX
Nonsmall cell lung cancer, response to tyrosine kinase inhibitor in211980Graph: Nonsmall cell lung cancer, response to tyrosine kinase inhibitor inMouseHumanRatWormXDictyXXXXYeastXX
Noonan syndrome 1163950Graph: Noonan syndrome 1MouseHumanXWormXXXXXXXXX
Noonan syndrome 3609942Graph: Noonan syndrome 3XXXWormXDictyXXXXXXX
Norum disease245900Graph: Norum diseaseXHumanXXXXXXXXYeastXX

O
OMIM disorder(s)OMIM_idComparisonGraphMouseHumanRatWormFlyDictyChickenZfinRiceTairYeastPombePfalc
Obesity, autosomal dominant601665Graph: Obesity, autosomal dominantMouseHumanRatXXXXXXXXXX
Obesity, mild, early-onset601665Graph: Obesity, mild, early-onsetMouseHumanRatXXXXXXXXXX
Obesity, severe601665Graph: Obesity, severeMouseHumanRatXXXXXXXXXX
Obestiy with impaired prohormone processing600955Graph: Obestiy with impaired prohormone processingXHumanXXXXXXXXXXX
Occipital horn syndrome304150Graph: Occipital horn syndromeMouseHumanXWormXXXXXXYeastXX
Oculocutaneous albinism, type IV606574Graph: Oculocutaneous albinism, type IVXXXXXXXXXXXXX
Oculodentodigital dysplasia164200Graph: Oculodentodigital dysplasiaMouseHumanRatXXXXZfinXXXXX
Oculofaciocardiodental syndrome300166Graph: Oculofaciocardiodental syndromeXHumanXXXXXXXXXXX
Oculopharyngeal muscular dystrophy164300Graph: Oculopharyngeal muscular dystrophyMouseHumanXWormXXXXXXXXX
Odontohypophosphatasia146300Graph: OdontohypophosphatasiaXXRatXXXXXXXYeastXX
Oguchi disease-1258100Graph: Oguchi disease-1XHumanRatXXXXXXXXXX
Oguchi disease-2258100Graph: Oguchi disease-2XHumanRatXXXXXXXXXX
Oligodendroglioma137800Graph: OligodendrogliomaMouseHumanRatWormXDictyXXXXXXX
Oligodontia604625Graph: OligodontiaMouseXXXXXXXXXXXX
Oligodontia-colorectal cancer syndrome608615Graph: Oligodontia-colorectal cancer syndromeMouseHumanRatXXXXXXXXXX
Omenn syndrome603554Graph: Omenn syndromeMouseHumanXXXXXXXXXXX
Optic atrophy 1165500Graph: Optic atrophy 1MouseHumanXWormXXXXXXXXX
Optic atrophy and cataract165300Graph: Optic atrophy and cataractXXXXXXXXXXXXX
Optic atrophy and deafness125250Graph: Optic atrophy and deafnessMouseHumanXWormXXXXXXXXX
Optic nerve coloboma with renal disease120330Graph: Optic nerve coloboma with renal diseaseMouseHumanXXXXXZfinXXXXX
Optic nerve hypoplasia/aplasia165550Graph: Optic nerve hypoplasia/aplasiaMouseHumanRatWormXXChickenXXXYeastXX
Oral-facial-digital syndrome 1311200Graph: Oral-facial-digital syndrome 1XXXXXXXXXXXXX
Ornithine transcarbamylase deficiency311250Graph: Ornithine transcarbamylase deficiencyMouseXXXXXChickenXXXYeastXX
Orofacial cleft 6608864Graph: Orofacial cleft 6XXXXXXXXXXXXX
Orthostatic intolerance604715Graph: Orthostatic intoleranceMouseHumanRatXXXXXXXXXX
Osseous heteroplasia, progressive166350Graph: Osseous heteroplasia, progressiveMouseXRatWormXXXXXXXXX
Ossification of posterior longitudinal ligament of spine602475Graph: Ossification of posterior longitudinal ligament of spineMouseHumanXXXXXXXXXXX
Osteoarthrosis165720Graph: OsteoarthrosisMouseHumanRatXXXXXXXXXX
Osteogenesis imperfecta, 3 clinical forms259420Graph: Osteogenesis imperfecta, 3 clinical formsXHumanXXXXXXXXXXX
Osteogenesis imperfecta, type I166200Graph: Osteogenesis imperfecta, type IXHumanXXXXXXXXXXX
Osteogenesis imperfecta, type II166210Graph: Osteogenesis imperfecta, type IIXHumanXXXXXXXXXXX
Osteogenesis imperfecta, type III259420Graph: Osteogenesis imperfecta, type IIIXHumanXXXXXXXXXXX
Osteogenesis imperfecta, type IV166220Graph: Osteogenesis imperfecta, type IVXHumanXXXXXXXXXXX
Osteolysis, familial expansile174810Graph: Osteolysis, familial expansileMouseHumanXXXXXXXXXXX
Osteolysis, idiopathic, Saudi type605156Graph: Osteolysis, idiopathic, Saudi typeXHumanRatXXXXXXXXXX
Osteopenia/osteoporosis166710Graph: Osteopenia/osteoporosisMouseHumanRatXXXXXXXXXX
Osteopetrosis, autosomal dominant, type I607634Graph: Osteopetrosis, autosomal dominant, type IMouseHumanXXXDictyXXXXXXX
Osteopetrosis, autosomal dominant, type II166600Graph: Osteopetrosis, autosomal dominant, type IIXXXXXXXXXXXXX
Osteopetrosis, autosomal recessive259700Graph: Osteopetrosis, autosomal recessiveMouseHumanXXXXXXXXYeastXX
Osteopetrosis, recessive259700Graph: Osteopetrosis, recessiveMouseHumanXXXXXXXXYeastXX
Osteoporosis166710Graph: OsteoporosisMouseHumanRatXXXXXXXXXX
Osteoporosis, idiopathic166710Graph: Osteoporosis, idiopathicMouseHumanRatXXXXXXXXXX
Osteoporosis, involutional166710Graph: Osteoporosis, involutionalMouseHumanRatXXXXXXXXXX
Osteoporosis-pseudoglioma syndrome259770Graph: Osteoporosis-pseudoglioma syndromeMouseHumanXXXDictyXXXXXXX
Osteosarcoma259500Graph: OsteosarcomaMouseHumanRatXXXXXXXYeastXX
Osteosarcoma, somatic259500Graph: Osteosarcoma, somaticMouseHumanRatXXXXXXXYeastXX
Otofaciocervical syndrome166780Graph: Otofaciocervical syndromeMouseHumanXXXXXXXXXXX
Otopalatodigital syndrome, type I311300Graph: Otopalatodigital syndrome, type IMouseHumanXXXDictyXXXXXXX
Otopalatodigital syndrome, type II304120Graph: Otopalatodigital syndrome, type IIMouseHumanXXXDictyXXXXXXX
Otospondylomegaepiphyseal dysplasia215150Graph: Otospondylomegaepiphyseal dysplasiaXXXXXXXXXXXXX
Ovarian cancer604370Graph: Ovarian cancerMouseHumanRatWormXDictyXXXXXXX
Ovarian dysgenesis 1233300Graph: Ovarian dysgenesis 1XHumanRatXXXXXXXXXX
Ovarian dysgenesis 2300510Graph: Ovarian dysgenesis 2XHumanRatXXXXXXXXXX
Ovarian hyperstimulation syndrome, gestational608115Graph: Ovarian hyperstimulation syndrome, gestationalXHumanRatXXXXXXXXXX
Ovarioleukodystrophy603896Graph: OvarioleukodystrophyMouseHumanRatWormXXXXXXYeastXX

P
OMIM disorder(s)OMIM_idComparisonGraphMouseHumanRatWormFlyDictyChickenZfinRiceTairYeastPombePfalc
PCWH609136Graph: PCWHMouseHumanRatXXXXZfinXXXXX
POR deficiency201750Graph: POR deficiencyMouseHumanXXXXXXXXYeastXX
PPM-X syndrome300055Graph: PPM-X syndromeXHumanXXXXXXXXXXX
Pachyonychia congenita, Jackson-Lawler type167210Graph: Pachyonychia congenita, Jackson-Lawler typeMouseHumanXXXXXXXXXXX
Pachyonychia congenita, Jadassohn-Lewandowsky type167200Graph: Pachyonychia congenita, Jadassohn-Lewandowsky typeMouseHumanXXXXXXXXXXX
Paget disease of bone602080Graph: Paget disease of boneMouseHumanXXXXXXXXXXX
Paget disease, juvenile239000Graph: Paget disease, juvenileMouseHumanRatXXXXXXXXXX
Pallidopontonigral degeneration168610Graph: Pallidopontonigral degenerationMouseHumanRatXXXXXXXXXX
Pallister-Hall syndrome146510Graph: Pallister-Hall syndromeMouseHumanRatXFlyXXXXXYeastXX
Palmoplantar keratoderma, nonepidermolytic600962Graph: Palmoplantar keratoderma, nonepidermolyticMouseHumanXXXXXXXXXXX
Palmoplantar verrucous nevus, unilateral144200Graph: Palmoplantar verrucous nevus, unilateralMouseHumanRatXXXXXXXXXX
Pancreatic agenesis260370Graph: Pancreatic agenesisMouseHumanRatWormXXXXXXXXX
Pancreatic cancer260350Graph: Pancreatic cancerMouseHumanRatWormXDictyXXXXXXX
Pancreatic cancer/melanoma syndrome606719Graph: Pancreatic cancer/melanoma syndromeXHumanXXXXXXXXXXX
Pancreatic carcinoma, somatic260350Graph: Pancreatic carcinoma, somaticMouseHumanRatWormXDictyXXXXXXX
Pancreatitis, hereditary167800Graph: Pancreatitis, hereditaryXHumanRatXXXXXXXXXX
Papillon-Lefevre syndrome245000Graph: Papillon-Lefevre syndromeXHumanRatXXXXXXXXXX
Paraganglioma, familial chromaffin, 4115310Graph: Paraganglioma, familial chromaffin, 4MouseHumanXWormXXXXXXYeastXX
Paragangliomas, familial nonchromaffin, 3605373Graph: Paragangliomas, familial nonchromaffin, 3MouseHumanXWormXXXXXXYeastXX
Paramyotonia congenita168300Graph: Paramyotonia congenitaXHumanXXXXXXXXXXX
Parathyroid adenoma with cystic changes145001Graph: Parathyroid adenoma with cystic changesXXXXXXXXXXXXX
Parathyroid carcinoma608266Graph: Parathyroid carcinomaXXXXXXXXXXXXX
Parietal foramina 1168500Graph: Parietal foramina 1MouseHumanXWormXXXXXXXXX
Parietal foramina 2609597Graph: Parietal foramina 2MouseXXWormXXXXXXYeastXX
Parietal foramina with cleidocranial dysplasia168550Graph: Parietal foramina with cleidocranial dysplasiaMouseHumanXWormXXXXXXXXX
Parkes Weber syndrome608355Graph: Parkes Weber syndromeMouseHumanXXXXXXXXXXX
Parkinson disease168600Graph: Parkinson diseaseMouseHumanRatWormXXXXXXYeastXPfalc
Parkinson disease 4, autosomal dominant Lewy body605543Graph: Parkinson disease 4, autosomal dominant Lewy bodyMouseHumanRatXXXXXXXXXX
Parkinson disease 7, autosomal recessive early-onset606324Graph: Parkinson disease 7, autosomal recessive early-onsetMouseHumanXXXXXXXXXXX
Parkinson disease, early onset605909Graph: Parkinson disease, early onsetMouseHumanXXXXXXXXXXX
Parkinson disease, familial168600Graph: Parkinson disease, familialMouseHumanRatWormXXXXXXYeastXPfalc
Parkinson disease, juvenile, type 2600116Graph: Parkinson disease, juvenile, type 2MouseHumanRatWormXXXXXXXXX
Partington syndrome309510Graph: Partington syndromeMouseXXXXXXXXXYeastXX
Pelger-Huet anomaly169400Graph: Pelger-Huet anomalyMouseHumanXXXXXXXXYeastXX
Pelizaeus-Merzbacher disease312080Graph: Pelizaeus-Merzbacher diseaseMouseXRatXXXXZfinXXXXX
Pelizaeus-Merzbacher-like disease, autosomal recessive608804Graph: Pelizaeus-Merzbacher-like disease, autosomal recessiveMouseXXXXXXXXXXXX
Pendred syndrome274600Graph: Pendred syndromeXHumanXXXXXXXXXXX
Periodic fever, familial142680Graph: Periodic fever, familialMouseHumanRatXXXXXXXXXX
Periodontitis, juvenile170650Graph: Periodontitis, juvenileXHumanRatXXXXXXXXXX
Periventricular heterotopia with microcephaly608097Graph: Periventricular heterotopia with microcephalyXHumanXXXXXXXXYeastXX
Persistent Mullerian duct syndrome, type I261550Graph: Persistent Mullerian duct syndrome, type IMouseHumanRatXXXXXXXXXX
Persistent Mullerian duct syndrome, type II261550Graph: Persistent Mullerian duct syndrome, type IIMouseHumanRatXXXXXXXXXX
Peters anomaly603807Graph: Peters anomalyMouseHumanRatWormXXChickenXXXYeastXX
Peutz-Jeghers syndrome175200Graph: Peutz-Jeghers syndromeXHumanXWormXXXXXXXXX
Pfeiffer syndrome101600Graph: Pfeiffer syndromeMouseHumanRatWormXXXXXXXXX
Phenylketonuria, atypical, due to GCH1 deficiency233910Graph: Phenylketonuria, atypical, due to GCH1 deficiencyXHumanRatXXDictyXXXXYeastXX
Pheochromocytoma171300Graph: PheochromocytomaMouseHumanRatWormXXXXXXYeastXX
Phosphoglycerate dehydrogenase deficiency601815Graph: Phosphoglycerate dehydrogenase deficiencyMouseHumanRatXXXXXXXYeastXX
Phosphorylase kinase deficiency of liver and muscle, autosomal recessive261750Graph: Phosphorylase kinase deficiency of liver and muscle, autosomal recessiveXHumanXXXXXXXXXXX
Pick disease172700Graph: Pick diseaseMouseHumanRatXXXXXXXXXX
Piebaldism172800Graph: PiebaldismMouseHumanRatXXXXXXTairXXX
Pigmented adrenocortical disease, primary isolated160980Graph: Pigmented adrenocortical disease, primary isolatedMouseHumanRatWormXDictyXXXXXXX
Pigmented paravenous chorioretinal atrophy172870Graph: Pigmented paravenous chorioretinal atrophyMouseHumanXXXXXXXXXXX
Pilomatricoma132600Graph: PilomatricomaMouseHumanRatWormXXXZfinXXXXX
Pituitary hormone deficiency, combined, HESX1-related182230Graph: Pituitary hormone deficiency, combined, HESX1-relatedMouseHumanXXXXXXXXXXX
Pituitary hormone deficiency, combined, with rigid cervical spine262600Graph: Pituitary hormone deficiency, combined, with rigid cervical spineXHumanXWormXXXXXXXXX
Platelet disorder, familial, with associated myeloid malignancy601399Graph: Platelet disorder, familial, with associated myeloid malignancyMouseHumanXXXXXXXXXXX
Platelet glycoprotein IV deficiency608404Graph: Platelet glycoprotein IV deficiencyXHumanRatXXXXXXXXXX
Pneumonitis, desquamative interstitial263000Graph: Pneumonitis, desquamative interstitialXXXXXXXXXXXXX
Pneumothorax, primary spontaneous173600Graph: Pneumothorax, primary spontaneousXXXXXXXXXXXXX
Polycystic kidney and hepatic disease263200Graph: Polycystic kidney and hepatic diseaseMouseXXXXXXXXXXXX
Polycystic kidney disease, adult type I173900Graph: Polycystic kidney disease, adult type IMouseHumanXXXXXXXXXXX
Polycystic liver disease174050Graph: Polycystic liver diseaseMouseXXXXXXXXXXXX
Polycystic ovary syndrome184700Graph: Polycystic ovary syndromeMouseHumanRatXXXXXXXXXX
Polycythemia, benign familial263400Graph: Polycythemia, benign familialMouseHumanRatXXXXXXXXXX
Polydactyly, postaxial, types A1 and B174200Graph: Polydactyly, postaxial, types A1 and BMouseHumanRatXFlyXXXXXYeastXX
Polydactyly, preaxial, type IV174700Graph: Polydactyly, preaxial, type IVMouseHumanRatXFlyXXXXXYeastXX
Polyposis syndrome, hereditary mixed, 2610069Graph: Polyposis syndrome, hereditary mixed, 2MouseHumanXWormXXXXXXXXX
Polyposis, juvenile intestinal174900Graph: Polyposis, juvenile intestinalMouseHumanXWormXXXXXXXXX
Popliteal pterygium syndrome119500Graph: Popliteal pterygium syndromeXXXXXXXXXXXXX
Porphyria variegata176200Graph: Porphyria variegataXHumanXXXXXXXXYeastXX
Porphyria, congenital erythropoietic263700Graph: Porphyria, congenital erythropoieticXHumanXXXXXXXXYeastXX
Prader-Willi syndrome176270Graph: Prader-Willi syndromeMouseHumanRatWormXXXXXXXXX
Precocious puberty, male176410Graph: Precocious puberty, maleMouseHumanXXXXXXXXXXX
Premature chromosome condensation with microcephaly and mental retardation606858Graph: Premature chromosome condensation with microcephaly and mental retardationXXXXXXXXXXXXX
Premature ovarian failure300511Graph: Premature ovarian failureMouseHumanXWormXXXXXXXXX
Premature ovarian failure 3608996Graph: Premature ovarian failure 3MouseXXXXXXXXXXXX
Primary lateral sclerosis, juvenile606353Graph: Primary lateral sclerosis, juvenileMouseHumanXXXXXXXXXXX
Prion disease with protracted course606688Graph: Prion disease with protracted courseMouseHumanRatXXXXXXXXXX
Progesterone resistance264080Graph: Progesterone resistanceMouseHumanRatXXXXXXXXXX
Progressive external ophthalmoplegia with mitochondrial DNA deletions157640Graph: Progressive external ophthalmoplegia with mitochondrial DNA deletionsMouseHumanRatWormXDictyXXXXYeastXX
Properdin deficiency, X-linked312060Graph: Properdin deficiency, X-linkedXHumanXXXXXXXXXXX
Propionicacidemia606054Graph: PropionicacidemiaMouseHumanRatXXXXXXXXXX
Prostate cancer176807Graph: Prostate cancerMouseHumanRatWormXXXXXXYeastXX
Prostate cancer 1601518Graph: Prostate cancer 1XHumanXXXXXXXXXXX
Prostate cancer, familial176807Graph: Prostate cancer, familialMouseHumanRatWormXXXXXXYeastXX
Prostate cancer, hereditary176807Graph: Prostate cancer, hereditaryMouseHumanRatWormXXXXXXYeastXX
Prostate cancer, progression and metastasis of176807Graph: Prostate cancer, progression and metastasis ofMouseHumanRatWormXXXXXXYeastXX
Prostate cancer, somatic176807Graph: Prostate cancer, somaticMouseHumanRatWormXXXXXXYeastXX
Proud syndrome300004Graph: Proud syndromeMouseXXXXXXXXXYeastXX
Pseudo-Zellweger syndrome261515Graph: Pseudo-Zellweger syndromeMouseHumanRatWormXDictyXXXXYeastXX
Pseudoachondroplasia177170Graph: PseudoachondroplasiaXHumanXXXXXXXXXXX
Pseudohermaphroditism, male, with gynecomastia264300Graph: Pseudohermaphroditism, male, with gynecomastiaXHumanRatXXXXXXXXXX
Pseudohypoaldosteronism type I, autosomal dominant177735Graph: Pseudohypoaldosteronism type I, autosomal dominantMouseHumanXXXXXXXXXXX
Pseudohypoaldosteronism, type I264350Graph: Pseudohypoaldosteronism, type IMouseHumanXWormXXXXXXXXX
Pseudohypoaldosteronism, type IIC145260Graph: Pseudohypoaldosteronism, type IICXHumanRatWormXXXXXXXXX
Pseudohypoparathyroidism, type Ia103580Graph: Pseudohypoparathyroidism, type IaMouseXRatWormXXXXXXXXX
Pseudohypoparathyroidism, type Ib603233Graph: Pseudohypoparathyroidism, type IbMouseXRatWormXXXXXXXXX
Pseudovaginal perineoscrotal hypospadias264600Graph: Pseudovaginal perineoscrotal hypospadiasMouseHumanRatXXXXXXXXXX
Pseudoxanthoma elasticum, autosomal dominant177850Graph: Pseudoxanthoma elasticum, autosomal dominantXHumanXXXXXXXXYeastXX
Pseudoxanthoma elasticum, autosomal recessive264800Graph: Pseudoxanthoma elasticum, autosomal recessiveXHumanXXXXXXXXYeastXX
Ptosis, congenital178300Graph: Ptosis, congenitalXXXXXXXXXXXXX
Pulmonary alveolar proteinosis265120Graph: Pulmonary alveolar proteinosisXHumanRatXXXXXXXXXX
Pulmonary alveolar proteinosis, congenital265120Graph: Pulmonary alveolar proteinosis, congenitalXHumanRatXXXXXXXXXX
Pulmonary fibrosis, idiopathic, familial178500Graph: Pulmonary fibrosis, idiopathic, familialXXXXXXXXXXXXX
Pycnodysostosis265800Graph: PycnodysostosisXHumanXXXXXXXXXXPfalc
Pyogenic sterile arthritis, pyoderma gangrenosum, and acne604416Graph: Pyogenic sterile arthritis, pyoderma gangrenosum, and acneMouseHumanXXXXXXXXXXX
Pyruvate carboxylase deficiency266150Graph: Pyruvate carboxylase deficiencyMouseHumanXXXXXXXXYeastXX

R
OMIM disorder(s)OMIM_idComparisonGraphMouseHumanRatWormFlyDictyChickenZfinRiceTairYeastPombePfalc
RAPADILINO syndrome266280Graph: RAPADILINO syndromeXHumanXXXXXXXXXXX
Rabson-Mendenhall syndrome262190Graph: Rabson-Mendenhall syndromeMouseHumanXWormXXChickenXXXXXX
Radioulnar synostosis with amegakaryocytic thrombocytopenia605432Graph: Radioulnar synostosis with amegakaryocytic thrombocytopeniaMouseHumanXXXXXXXXXXX
Rapp-Hodgkin syndrome129400Graph: Rapp-Hodgkin syndromeMouseHumanRatXXXXXXXXXX
Refsum disease266500Graph: Refsum diseaseMouseHumanRatXXXXXXXYeastXX
Refsum disease, infantile266510Graph: Refsum disease, infantileMouseHumanRatWormXXXXXXYeastXX
Refsum disease, infantile form266510Graph: Refsum disease, infantile formMouseHumanRatWormXXXXXXYeastXX
Renal carcinoma, chromophobe, somatic144700Graph: Renal carcinoma, chromophobe, somaticMouseHumanRatXXXXXXXYeastXX
Renal cell carcinoma144700Graph: Renal cell carcinomaMouseHumanRatXXXXXXXYeastXX
Renal cell carcinoma, clear cell, somatic144700Graph: Renal cell carcinoma, clear cell, somaticMouseHumanRatXXXXXXXYeastXX
Renal cell carcinoma, papillary, 1605074Graph: Renal cell carcinoma, papillary, 1MouseHumanRatXXXXXXXXXX
Renal cell carcinoma, papillary, familial and sporadic605074Graph: Renal cell carcinoma, papillary, familial and sporadicMouseHumanRatXXXXXXXXXX
Renal cell carcinoma, somatic144700Graph: Renal cell carcinoma, somaticMouseHumanRatXXXXXXXYeastXX
Renal cysts and diabetes syndrome137920Graph: Renal cysts and diabetes syndromeMouseHumanRatXXXXZfinXXXXX
Renal glucosuria233100Graph: Renal glucosuriaXHumanXXXXXXXXXXX
Renal tubular acidosis with deafness267300Graph: Renal tubular acidosis with deafnessMouseXXWormXXXXXXYeastXX
Renal tubular acidosis, distal602722Graph: Renal tubular acidosis, distalMouseHumanXWormXXXXXXYeastXX
Renal tubular acidosis, distal, autosomal recessive602722Graph: Renal tubular acidosis, distal, autosomal recessiveMouseHumanXWormXXXXXXYeastXX
Renal tubular acidosis, proximal, with ocular abnormalities604278Graph: Renal tubular acidosis, proximal, with ocular abnormalitiesMouseXRatXXXXXXXXXX
Renal tubular dysgenesis267430Graph: Renal tubular dysgenesisMouseHumanRatWormXXXXXXYeastXPfalc
Renpenning syndrome309500Graph: Renpenning syndromeXHumanXXXXXXXXXXX
Restrictive dermopathy, lethal275210Graph: Restrictive dermopathy, lethalMouseHumanXXXXXXXXYeastXX
Retinitis pigmentosa, AR268000Graph: Retinitis pigmentosa, ARMouseHumanRatXXXXXXXXXX
Retinitis pigmentosa, AR, without hearing loss268000Graph: Retinitis pigmentosa, AR, without hearing lossMouseHumanRatXXXXXXXXXX
Retinitis pigmentosa, MERTK-related268000Graph: Retinitis pigmentosa, MERTK-relatedMouseHumanRatXXXXXXXXXX
Retinitis pigmentosa, X-linked with deafness and sinorespiratory infections300455Graph: Retinitis pigmentosa, X-linked with deafness and sinorespiratory infectionsMouseHumanXXXXXXXXXXX
Retinitis pigmentosa, X-linked, with recurrent respiratory infections300455Graph: Retinitis pigmentosa, X-linked, with recurrent respiratory infectionsMouseHumanXXXXXXXXXXX
Retinitis pigmentosa, autosomal recessive268000Graph: Retinitis pigmentosa, autosomal recessiveMouseHumanRatXXXXXXXXXX
Retinitis pigmentosa, digenic608133Graph: Retinitis pigmentosa, digenicXHumanXXXXXXXXXXX
Retinitis pigmentosa, late onset268000Graph: Retinitis pigmentosa, late onsetMouseHumanRatXXXXXXXXXX
Retinitis pigmentosa, late-onset dominant268000Graph: Retinitis pigmentosa, late-onset dominantMouseHumanRatXXXXXXXXXX
Retinitis pigmentosa-1180100Graph: Retinitis pigmentosa-1MouseHumanXXXXXXXXXXX
Retinitis pigmentosa-10180105Graph: Retinitis pigmentosa-10MouseHumanXXXXXXXXYeastXX
Retinitis pigmentosa-11600138Graph: Retinitis pigmentosa-11XHumanXXXXXXXXYeastXX
Retinitis pigmentosa-12, autosomal recessive600105Graph: Retinitis pigmentosa-12, autosomal recessiveMouseHumanXXXXXXXXXXX
Retinitis pigmentosa-13600059Graph: Retinitis pigmentosa-13XHumanXWormXXXXXXYeastXX
Retinitis pigmentosa-14600132Graph: Retinitis pigmentosa-14MouseHumanXXFlyXXXXXXXX
Retinitis pigmentosa-17600852Graph: Retinitis pigmentosa-17XHumanXXXXXXXXXXX
Retinitis pigmentosa-18601414Graph: Retinitis pigmentosa-18XXXXXXXXXXYeastXX
Retinitis pigmentosa-19601718Graph: Retinitis pigmentosa-19MouseHumanXXXXXXXXXXX
Retinitis pigmentosa-26608380Graph: Retinitis pigmentosa-26XXXXXXXXXXXXX
Retinitis pigmentosa-3300389Graph: Retinitis pigmentosa-3MouseHumanXXXXXXXXXXX
Retinitis pigmentosa-30607921Graph: Retinitis pigmentosa-30XHumanXXXXXXXXXXX
Retinitis pigmentosa-7608133Graph: Retinitis pigmentosa-7XHumanXXXXXXXXXXX
Retinitis pigmentosa-9180104Graph: Retinitis pigmentosa-9XXXXXXXXXXXXX
Retinitis punctata albescens136880Graph: Retinitis punctata albescensMouseHumanXXXXXXXXXXX
Rett syndrome312750Graph: Rett syndromeXHumanXXXXXXXXXXX
Rett syndrome, preserved speech variant312750Graph: Rett syndrome, preserved speech variantXHumanXXXXXXXXXXX
Rhabdomyosarcoma268210Graph: RhabdomyosarcomaMouseXXXXXXXXXXXX
Rhabdomyosarcoma, alveolar268220Graph: Rhabdomyosarcoma, alveolarMouseHumanRatWormXXXXXXYeastXX
Rhizomelic chondrodysplasia punctata, type 1215100Graph: Rhizomelic chondrodysplasia punctata, type 1MouseHumanXXXXXXXXYeastXX
Rhizomelic chondrodysplasia punctata, type 3600121Graph: Rhizomelic chondrodysplasia punctata, type 3XHumanXWormXXXXXXXXX
Ribose 5-phosphate isomerase deficiency608611Graph: Ribose 5-phosphate isomerase deficiencyXXXXXDictyXXXXYeastXX
Rickets due to defect in vitamin D 25-hydroxylation600081Graph: Rickets due to defect in vitamin D 25-hydroxylationMouseXXXXXXXXXXXX
Rickets, vitamin D-resistant, type IIA277440Graph: Rickets, vitamin D-resistant, type IIAMouseHumanRatXXXXXXXXXX
Rieger syndrome180500Graph: Rieger syndromeMouseHumanXXXXXXXXYeastXX
Ring dermoid of cornea180550Graph: Ring dermoid of corneaMouseHumanXXXXXXXXYeastXX
Rippling muscle disease606072Graph: Rippling muscle diseaseMouseHumanRatWormXXXXXXXXX
Robinow syndrome, autosomal recessive268310Graph: Robinow syndrome, autosomal recessiveMouseHumanXWormXXXXXXXXX
Rokitansky-Kuster-Hauser syndrome277000Graph: Rokitansky-Kuster-Hauser syndromeMouseXXXXXXXXXXXX
Rothmund-Thomson syndrome268400Graph: Rothmund-Thomson syndromeXHumanXXXXXXXXXXX
Roussy-Levy syndrome180800Graph: Roussy-Levy syndromeMouseHumanRatXXXXXXXXXX
Rubenstein-Taybi syndrome180849Graph: Rubenstein-Taybi syndromeMouseHumanRatWormXXXXXXXXX
Rubinstein-Taybi syndrome180849Graph: Rubinstein-Taybi syndromeMouseHumanRatWormXXXXXXXXX

S
OMIM disorder(s)OMIM_idComparisonGraphMouseHumanRatWormFlyDictyChickenZfinRiceTairYeastPombePfalc
SMED Strudwick type184250Graph: SMED Strudwick typeMouseHumanRatXXXXXXXXXX
Saccharopinuria268700Graph: SaccharopinuriaMouseHumanXXXXXXXXYeastXX
Saethre-Chotzen syndrome101400Graph: Saethre-Chotzen syndromeMouseXXWormXXXXXXXXX
Saethre-Chotzen syndrome with eyelid anomalies101400Graph: Saethre-Chotzen syndrome with eyelid anomaliesMouseXXWormXXXXXXXXX
Salla disease604369Graph: Salla diseaseMouseHumanXXXXXXXXXXX
Sandhoff disease, infantile, juvenile, and adult forms268800Graph: Sandhoff disease, infantile, juvenile, and adult formsMouseHumanXXXXXXXXXXX
Sanfilippo syndrome, type A252900Graph: Sanfilippo syndrome, type AMouseHumanXXXXXXXXXXX
Sarcoidosis, early-onset181000Graph: Sarcoidosis, early-onsetMouseHumanXXXXXXXXXXX
Schimke immunoosseous dysplasia242900Graph: Schimke immunoosseous dysplasiaMouseXXXXXXXXXXXX
Schindler disease, type I609241Graph: Schindler disease, type IXHumanXXXXXXXXXXX
Schindler disease, type III609241Graph: Schindler disease, type IIIXHumanXXXXXXXXXXX
Schizencephaly269160Graph: SchizencephalyMouseHumanXXXXXXXXXXX
Schwannomatosis162091Graph: SchwannomatosisMouseHumanXXXXXXXXXXX
Schwartz-Jampel syndrome, type 1255800Graph: Schwartz-Jampel syndrome, type 1MouseXXWormXXXXXXXXX
Sclerosteosis269500Graph: SclerosteosisMouseHumanXXXXXXXXXXX
Sea-blue histiocyte disease269600Graph: Sea-blue histiocyte diseaseMouseHumanRatXXXXXXXXXX
Sebastian syndrome605249Graph: Sebastian syndromeMouseXXWormXDictyXXXXYeastPombeX
Seckel syndrome 1210600Graph: Seckel syndrome 1MouseHumanXXXXXXXXYeastXX
Self-healing collodion baby242300Graph: Self-healing collodion babyMouseHumanXXXXXXXXXXX
Senior-Loken syndrome-1266900Graph: Senior-Loken syndrome-1XHumanXXXXXXXXXXX
Sensory ataxia neuropathy, dysarthria, and ophthalmoparesis607459Graph: Sensory ataxia neuropathy, dysarthria, and ophthalmoparesisMouseHumanRatXXXXXXXYeastXX
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis607459Graph: Sensory ataxic neuropathy, dysarthria, and ophthalmoparesisMouseHumanRatXXXXXXXYeastXX
Septooptic dysplasia182230Graph: Septooptic dysplasiaMouseHumanXXXXXXXXXXX
Sertoli-cell-only syndrome415000Graph: Sertoli-cell-only syndromeMouseHumanRatXXXXXXXXXX
Severe combined immunodeficiency, Athabascan type602450Graph: Severe combined immunodeficiency, Athabascan typeMouseXXXXXXXXXXXX
Severe combined immunodeficiency, B cell-negative601457Graph: Severe combined immunodeficiency, B cell-negativeMouseHumanXXXXXXXXXXX
Severe combined immunodeficiency, T-cell negative, B-cell/natural killer cell-positive type600802Graph: Severe combined immunodeficiency, T-cell negative, B-cell/natural killer cell-positive typeMouseHumanXXXXXXXXXXX
Severe combined immunodeficiency, T-negative/B-positive type600802Graph: Severe combined immunodeficiency, T-negative/B-positive typeMouseHumanXXXXXXXXXXX
Severe combined immunodeficiency, X-linked300400Graph: Severe combined immunodeficiency, X-linkedMouseHumanRatXXXXXXXXXX
Severe combined immunodeficiency, type I202500Graph: Severe combined immunodeficiency, type IMouseHumanXXXXXXXXXXX
Shah-Waardenburg syndrome277580Graph: Shah-Waardenburg syndromeMouseHumanRatXXXXZfinXXXXX
Short QT syndrome-1609620Graph: Short QT syndrome-1MouseHumanRatXXXXXXXXXX
Short QT syndrome-2609621Graph: Short QT syndrome-2MouseHumanRatXXXXXXXXXX
Short QT syndrome-3609622Graph: Short QT syndrome-3XHumanXXXXXXXXXXX
Short stature, idiopathic familial604271Graph: Short stature, idiopathic familialXXXXXXXXXXXXX
Short stature, pituitary and cerebellar defects, and small sella turcica606606Graph: Short stature, pituitary and cerebellar defects, and small sella turcicaMouseXXWormXXXXXXXXX
Shprintzen-Goldberg syndrome182212Graph: Shprintzen-Goldberg syndromeMouseHumanXWormXXXXXXXXX
Shwachman-Diamond syndrome260400Graph: Shwachman-Diamond syndromeXHumanXXXXXXXXYeastXX
Sialic acid storage disorder, infantile269920Graph: Sialic acid storage disorder, infantileMouseHumanXXXXXXXXXXX
Sialidosis, type I256550Graph: Sialidosis, type IXHumanXXXXXXXXXXX
Sialidosis, type II256550Graph: Sialidosis, type IIXHumanXXXXXXXXXXX
Sialuria269921Graph: SialuriaMouseHumanRatXXXXXXXXXX
Sick sinus syndrome608567Graph: Sick sinus syndromeXHumanRatXXXXXXXXXX
Silver spastic paraplegia syndrome270685Graph: Silver spastic paraplegia syndromeXHumanXXXXXXXXXXX
Simpson-Golabi-Behmel syndrome, type 1312870Graph: Simpson-Golabi-Behmel syndrome, type 1MouseHumanXXXXXZfinXXXXX
Sitosterolemia210250Graph: SitosterolemiaXXRatXXXXXXXXXX
Situs inversus viscerum270100Graph: Situs inversus viscerumMouseXXXXXXXXXXXX
Skin fragility-woolly hair syndrome607655Graph: Skin fragility-woolly hair syndromeXHumanXXXXXXXXXXX
Slowed nerve conduction velocity, AD608236Graph: Slowed nerve conduction velocity, ADXXXXXXXXXXXXX
Small patella syndrome147891Graph: Small patella syndromeMouseHumanXXXXXXXXXXX
Smith-Fineman-Myers syndrome309580Graph: Smith-Fineman-Myers syndromeMouseHumanRatWormXXXXXXXXX
Smith-Lemli-Opitz syndrome270400Graph: Smith-Lemli-Opitz syndromeMouseHumanRatXFlyXXXXXXXX
Smith-Magenis syndrome182290Graph: Smith-Magenis syndromeMouseHumanXXXXXXXXXXX
Smith-McCort dysplasia607326Graph: Smith-McCort dysplasiaXXXXXXXXXXXXX
Solitary median maxillary central incisor147250Graph: Solitary median maxillary central incisorMouseHumanRatWormXXXXXXXXX
Sorsby fundus dystrophy136900Graph: Sorsby fundus dystrophyMouseXRatXXXXXXXXXX
Sotos syndrome117550Graph: Sotos syndromeMouseHumanXWormXXXXXXXXX
Spastic ataxia, Charlevoix-Saguenay type270550Graph: Spastic ataxia, Charlevoix-Saguenay typeXXXXXXXXXXXXX
Spastic paralysis, infantile onset ascending607225Graph: Spastic paralysis, infantile onset ascendingMouseHumanXXXXXXXXXXX
Spastic paraplegia 10604187Graph: Spastic paraplegia 10MouseHumanXWormXXXXXXXXX
Spastic paraplegia-13605280Graph: Spastic paraplegia-13MouseHumanXWormXXXXXXYeastXX
Spastic paraplegia-2312920Graph: Spastic paraplegia-2MouseXRatXXXXZfinXXXXX
Spastic paraplegia-3A182600Graph: Spastic paraplegia-3AXXXXXXXXXXXXX
Spastic paraplegia-4182601Graph: Spastic paraplegia-4XHumanXXXXXXXXYeastXX
Spastic paraplegia-7607259Graph: Spastic paraplegia-7MouseHumanXXXXXXXXXXX
Speech-language disorder-1602081Graph: Speech-language disorder-1MouseXXXXXXXXXXXX
Spina bifida601634Graph: Spina bifidaMouseXRatXXXXXXXYeastXX
Spinal and bulbar muscular atrophy of Kennedy313200Graph: Spinal and bulbar muscular atrophy of KennedyMouseHumanRatXXXXXXXXXX
Spinal muscular atrophy with respiratory distress604320Graph: Spinal muscular atrophy with respiratory distressMouseHumanRatXXXXXXXYeastXX
Spinal muscular atrophy, distal, type V600794Graph: Spinal muscular atrophy, distal, type VMouseHumanXWormXXXXXXYeastXX
Spinal muscular atrophy, late-onset, Finkel type182980Graph: Spinal muscular atrophy, late-onset, Finkel typeXHumanXXXXXXXXYeastXX
Spinal muscular atrophy-1253300Graph: Spinal muscular atrophy-1MouseXXWormXXXZfinXXXXX
Spinal muscular atrophy-2253550Graph: Spinal muscular atrophy-2MouseXXWormXXXZfinXXXXX
Spinal muscular atrophy-3253400Graph: Spinal muscular atrophy-3MouseXXWormXXXZfinXXXXX
Spinal muscular atrophy-4271150Graph: Spinal muscular atrophy-4MouseXXWormXXXZfinXXXXX
Spinocerebellar ataxia 12604326Graph: Spinocerebellar ataxia 12XHumanRatWormXXXXXXYeastXX
Spinocerebellar ataxia 14605361Graph: Spinocerebellar ataxia 14MouseHumanRatXXXXXXXYeastXX
Spinocerebellar ataxia 17607136Graph: Spinocerebellar ataxia 17MouseHumanXWormXXXXXXYeastXPfalc
Spinocerebellar ataxia with epilepsy607459Graph: Spinocerebellar ataxia with epilepsyMouseHumanRatXXXXXXXYeastXX
Spinocerebellar ataxia, autosomal recessive with axonal neuropathy607250Graph: Spinocerebellar ataxia, autosomal recessive with axonal neuropathyXXXXXXXXXXYeastXX
Spinocerebellar ataxia-1164400Graph: Spinocerebellar ataxia-1XHumanXXXXXXXXXXX
Spinocerebellar ataxia-27609307Graph: Spinocerebellar ataxia-27XHumanRatXXXXXXXXXX
Spinocerebellar ataxia-6183086Graph: Spinocerebellar ataxia-6MouseHumanRatXXXXXXXXXX
Spinocerebellar ataxia-7164500Graph: Spinocerebellar ataxia-7XHumanXXXXXXXXXXX
Split hand/foot malformation, type 3600095Graph: Split hand/foot malformation, type 3XXXXXXXXXXXXX
Split-hand/foot malformation, type 4605289Graph: Split-hand/foot malformation, type 4MouseHumanRatXXXXXXXXXX
Spondylocarpotarsal synostosis syndrome272460Graph: Spondylocarpotarsal synostosis syndromeMouseHumanXXXDictyXXXXXXX
Spondylocostal dysostosis, autosomal recessive, 1277300Graph: Spondylocostal dysostosis, autosomal recessive, 1MouseHumanRatXXXXXXXXXX
Spondyloepimetaphyseal dysplasia608728Graph: Spondyloepimetaphyseal dysplasiaMouseHumanXXXXXXXXXXX
Spondyloepiphyseal dysplasia tarda313400Graph: Spondyloepiphyseal dysplasia tardaXXXXXXXXXTairYeastXX
Spondyloepiphyseal dysplasia tarda with progressive arthropathy208230Graph: Spondyloepiphyseal dysplasia tarda with progressive arthropathyXHumanXXFlyXXXXXXXX
Spondyloepiphyseal dysplasia, Omani type608637Graph: Spondyloepiphyseal dysplasia, Omani typeXHumanXXXXXXXXXXX
Squamous cell carcinoma, head and neck275355Graph: Squamous cell carcinoma, head and neckXHumanXXXXXXXXYeastXX
Stapes ankylosis syndrome without symphalangism184460Graph: Stapes ankylosis syndrome without symphalangismMouseHumanRatXXXXZfinXXXXX
Stargardt disease 3600110Graph: Stargardt disease 3XXXXXXXXXXYeastXX
Stargardt disease-1248200Graph: Stargardt disease-1MouseHumanXXXXXXXXXXX
Startle disease/hyperekplexia, autosomal dominant149400Graph: Startle disease/hyperekplexia, autosomal dominantXHumanRatWormXXXXXXXXX
Steatocystoma multiplex184500Graph: Steatocystoma multiplexMouseHumanXXXXXXXXXXX
Stickler syndrome, type I108300Graph: Stickler syndrome, type IMouseHumanRatXXXXXXXXXX
Stickler syndrome, type II604841Graph: Stickler syndrome, type IIMouseHumanXXXXXXXXXXX
Stickler syndrome, type III184840Graph: Stickler syndrome, type IIIXXXXXXXXXXXXX
Stomach cancer137215Graph: Stomach cancerMouseHumanRatWormFlyDictyXXXXXXX
Stomatocytosis I185000Graph: Stomatocytosis IXXXWormXXXXXXXXX
Stuve-Wiedemann syndrome/Schwartz-Jampel type 2 syndrome601559Graph: Stuve-Wiedemann syndrome/Schwartz-Jampel type 2 syndromeMouseHumanXXXXXXXXXXX
Subcortical laminal heteropia, X-linked300067Graph: Subcortical laminal heteropia, X-linkedMouseHumanXWormXXXXXXXXX
Sudden infant death with dysgenesis of the testes syndrome608800Graph: Sudden infant death with dysgenesis of the testes syndromeXXXXXXXXXXXXX
Sulfite oxidase deficiency272300Graph: Sulfite oxidase deficiencyMouseHumanRatXXXXXXXXXX
Supranuclear palsy, progressive601104Graph: Supranuclear palsy, progressiveMouseHumanRatXXXXXXXXXX
Supranuclear palsy, progressive atypical260540Graph: Supranuclear palsy, progressive atypicalMouseHumanRatXXXXXXXXXX
Supravalvar aortic stenosis185500Graph: Supravalvar aortic stenosisMouseHumanRatXXXXXXXXXX
Surfactant deficiency, neonatal267450Graph: Surfactant deficiency, neonatalXHumanXXXXXXXXXXX
Sutherland-Haan syndrome-like300465Graph: Sutherland-Haan syndrome-likeMouseHumanRatWormXXXXXXXXX
Symphalangism, proximal185800Graph: Symphalangism, proximalMouseHumanRatXXXXZfinXXXXX
Syndactyly, type III186100Graph: Syndactyly, type IIIMouseHumanRatXXXXZfinXXXXX
Syndactyly, type V186300Graph: Syndactyly, type VMouseHumanXXXXXXXXXXX
Synostoses syndrome, multiple, 1186500Graph: Synostoses syndrome, multiple, 1MouseHumanRatXXXXZfinXXXXX
Synpolydactyly with foot anomalies186000Graph: Synpolydactyly with foot anomaliesMouseHumanXXXXXXXXXXX
Synpolydactyly, 3/3'4, associated with metacarpal and metatarsal synostoses608180Graph: Synpolydactyly, 3/3'4, associated with metacarpal and metatarsal synostosesMouseHumanXWormXXXXXXXXX
Synpolydactyly, type II186000Graph: Synpolydactyly, type IIMouseHumanXXXXXXXXXXX

T
OMIM disorder(s)OMIM_idComparisonGraphMouseHumanRatWormFlyDictyChickenZfinRiceTairYeastPombePfalc
Tangier disease205400Graph: Tangier diseaseMouseHumanRatXXXXXXXXXX
Tarsal-carpal coalition syndrome186570Graph: Tarsal-carpal coalition syndromeMouseHumanRatXXXXZfinXXXXX
Tay-Sachs disease272800Graph: Tay-Sachs diseaseMouseHumanXXXXXXXXXXX
Tetra-amelia, autosomal recessive273395Graph: Tetra-amelia, autosomal recessiveMouseXXXXXXXXXXXX
Tetralogy of Fallot187500Graph: Tetralogy of FallotMouseHumanRatWormXXXZfinXXXXX
Tetrology of Fallot187500Graph: Tetrology of FallotMouseHumanRatWormXXXZfinXXXXX
Thalassemia-beta, dominant inclusion-body603902Graph: Thalassemia-beta, dominant inclusion-bodyXXXXXXXXXXXXX
Thanatophoric dysplasia, types I and II187600Graph: Thanatophoric dysplasia, types I and IIMouseHumanXWormXXXXXXXXX
Thiamine-responsive megaloblastic anemia syndrome249270Graph: Thiamine-responsive megaloblastic anemia syndromeMouseHumanXXXXXXXXXXX
Thrombocythemia, essential187950Graph: Thrombocythemia, essentialMouseHumanRatXXXXXXXXXX
Thrombocytopenia, X-linked313900Graph: Thrombocytopenia, X-linkedMouseHumanXXXDictyXXXXYeastXX
Thrombocytopenia, X-linked, intermittent313900Graph: Thrombocytopenia, X-linked, intermittentMouseHumanXXXDictyXXXXYeastXX
Thrombocytopenia, congenital amegakaryocytic604498Graph: Thrombocytopenia, congenital amegakaryocyticXHumanXXXXXXXXXXX
Thrombocytopenia-2188000Graph: Thrombocytopenia-2XXXXXXXXXXXXX
Thrombotic thrombocytopenic purpura, familial274150Graph: Thrombotic thrombocytopenic purpura, familialXHumanXXXXXXXXXXX
Thyroid carcinoma, follicular188470Graph: Thyroid carcinoma, follicularMouseHumanRatWormXDictyXXXXXXX
Thyroid carcinoma, papillary188550Graph: Thyroid carcinoma, papillaryMouseHumanRatWormXDictyXXXXXXX
Thyroid hormone organification defect IIA274500Graph: Thyroid hormone organification defect IIAXHumanXXXXXXXXXXX
Thyroid hormone resistance188570Graph: Thyroid hormone resistanceMouseHumanRatWormXXXXXXXXX
Thyroid hormone resistance, autosomal recessive274300Graph: Thyroid hormone resistance, autosomal recessiveMouseHumanRatWormXXXXXXXXX
Thyroid papillary carcinoma188550Graph: Thyroid papillary carcinomaMouseHumanRatWormXDictyXXXXXXX
Tibial muscular dystrophy, tardive600334Graph: Tibial muscular dystrophy, tardiveMouseHumanRatWormXXXXXXXXPfalc
Tietz syndrome103500Graph: Tietz syndromeXHumanXXXXXXXXXXX
Timothy syndrome601005Graph: Timothy syndromeMouseHumanRatWormXXXXXXXXX
Toenail dystrophy, isolated607523Graph: Toenail dystrophy, isolatedXHumanXXXXXXXXXXX
Total iodide organification defect274500Graph: Total iodide organification defectXHumanXXXXXXXXXXX
Townes-Brocks branchiootorenal-like syndrome107480Graph: Townes-Brocks branchiootorenal-like syndromeMouseHumanXWormXXChickenXXXXXX
Townes-Brocks syndrome107480Graph: Townes-Brocks syndromeMouseHumanXWormXXChickenXXXXXX
Transaldolase deficiency606003Graph: Transaldolase deficiencyXHumanXXXXXXXXYeastXX
Transient bullous of the newborn131705Graph: Transient bullous of the newbornXHumanXXXXXXXXXXX
Transposition of great arteries, dextro-looped217095Graph: Transposition of great arteries, dextro-loopedXHumanXWormXXXXXXXXX
Transposition of the great arteries, dextro-looped608808Graph: Transposition of the great arteries, dextro-loopedMouseXXWormXXXXXXXXX
Treacher Collins mandibulofacial dysostosis154500Graph: Treacher Collins mandibulofacial dysostosisMouseHumanXXXXXXXXXXX
Trichodontoosseous syndrome190320Graph: Trichodontoosseous syndromeXHumanXWormXXXZfinXXXXX
Trichorhinophalangeal syndrome, type I190350Graph: Trichorhinophalangeal syndrome, type IXHumanXXXXXXXXXXX
Trichorhinophalangeal syndrome, type III190351Graph: Trichorhinophalangeal syndrome, type IIIXHumanXXXXXXXXXXX
Trichothiodystrophy601675Graph: TrichothiodystrophyMouseHumanXXXXXXXXYeastXX
Trismus-pseudocomptodactyly syndrome158300Graph: Trismus-pseudocomptodactyly syndromeXHumanXWormXDictyXXXXYeastPombeX
Tropical calcific pancreatitis608189Graph: Tropical calcific pancreatitisXXXXXXXXXXXXX
Troyer syndrome275900Graph: Troyer syndromeXXXXXXXXXXXXX
Tuberous sclerosis-1191100Graph: Tuberous sclerosis-1MouseHumanRatXXXXXXXXXX
Tuberous sclerosis-2191100Graph: Tuberous sclerosis-2MouseHumanRatXXXXXXXXXX
Turcot syndrome276300Graph: Turcot syndromeMouseHumanRatWormFlyXXXXXYeastXX
Turcot syndrome with glioblastoma276300Graph: Turcot syndrome with glioblastomaMouseHumanRatWormFlyXXXXXYeastXX
Twinning, dizygotic276400Graph: Twinning, dizygoticXHumanRatXXXXXXXXXX

U
OMIM disorder(s)OMIM_idComparisonGraphMouseHumanRatWormFlyDictyChickenZfinRiceTairYeastPombePfalc
Ullrich congenital muscular dystrophy254090Graph: Ullrich congenital muscular dystrophyMouseHumanXXXXXXXXXXX
Ulnar-mammary syndrome181450Graph: Ulnar-mammary syndromeXHumanXWormXXXXXXXXX
Unna-Thost disease, nonepidermolytic600962Graph: Unna-Thost disease, nonepidermolyticMouseHumanXXXXXXXXXXX
Usher syndrome, type 1B276900Graph: Usher syndrome, type 1BMouseHumanRatXXDictyXXXXXXX
Usher syndrome, type 1C276904Graph: Usher syndrome, type 1CMouseXRatXXXXXXXXXX
Usher syndrome, type 1D601067Graph: Usher syndrome, type 1DMouseXRatXXXXXXXXXX
Usher syndrome, type 1F602083Graph: Usher syndrome, type 1FMouseXXXXXXZfinXXXXX
Usher syndrome, type 1G606943Graph: Usher syndrome, type 1GXXXXXXXXXXXXX
Usher syndrome, type 2A276901Graph: Usher syndrome, type 2AXHumanXXXXXXXXXXX
Usher syndrome, type 3276902Graph: Usher syndrome, type 3XXXXXXXXXXXXX
Usher syndrome, type IIC605472Graph: Usher syndrome, type IICMouseHumanXXXXXXXXXXX

V
OMIM disorder(s)OMIM_idComparisonGraphMouseHumanRatWormFlyDictyChickenZfinRiceTairYeastPombePfalc
VATER association with hydrocephalus276950Graph: VATER association with hydrocephalusMouseHumanRatWormXDictyXXXXXXX
Van Buchem disease239100Graph: Van Buchem diseaseMouseHumanXXXXXXXXXXX
Velocardiofacial syndrome192430Graph: Velocardiofacial syndromeXHumanXWormXXXXXXXXX
Venous malformations, multiple cutaneous and mucosal600195Graph: Venous malformations, multiple cutaneous and mucosalMouseHumanXXXXXXXXXXX
Ventricular fibrillation, idiopathic603829Graph: Ventricular fibrillation, idiopathicXHumanRatXXXXXXXXXX
Ventricular tachycardia, idiopathic192605Graph: Ventricular tachycardia, idiopathicMouseHumanRatXXDictyXXRiceXYeastXX
Ventricular tachycardia, stress-induced polymorphic604772Graph: Ventricular tachycardia, stress-induced polymorphicMouseHumanXWormXXXXXXXXX
Vertical talus, congenital192950Graph: Vertical talus, congenitalXHumanXXXXXXXXXXX
Vitamin K-dependent clotting factors, combined deficiency of, 2607473Graph: Vitamin K-dependent clotting factors, combined deficiency of, 2MouseXRatXXXXXXXXXX
Vitamin K-dependent coagulation defect277450Graph: Vitamin K-dependent coagulation defectXHumanXXXXXXXXXXX
Vitelliform macular dystrophy, adult-onset608161Graph: Vitelliform macular dystrophy, adult-onsetXHumanXXXXXXXXXXX
Vohwinkel syndrome124500Graph: Vohwinkel syndromeMouseHumanRatXXXXXXXXXX

W
OMIM disorder(s)OMIM_idComparisonGraphMouseHumanRatWormFlyDictyChickenZfinRiceTairYeastPombePfalc
WAGR syndrome194072Graph: WAGR syndromeMouseXXXXXXXXXXXX
WHIM syndrome193670Graph: WHIM syndromeMouseXRatXXXXXXXXXX
Waardenburg syndrome, type I193500Graph: Waardenburg syndrome, type IMouseHumanXXXXXXXXYeastXX
Waardenburg syndrome, type IIA193510Graph: Waardenburg syndrome, type IIAXHumanXXXXXXXXXXX
Waardenburg syndrome, type IID608890Graph: Waardenburg syndrome, type IIDMouseHumanRatXXXXXXTairXXX
Waardenburg syndrome, type III148820Graph: Waardenburg syndrome, type IIIMouseHumanXXXXXXXXYeastXX
Waardenburg syndrome/albinism, digenic103470Graph: Waardenburg syndrome/albinism, digenicMouseHumanXXXXXXXXXXX
Waardenburg syndrome/ocular albinism, digenic103470Graph: Waardenburg syndrome/ocular albinism, digenicMouseHumanXXXXXXXXXXX
Waardenburg-Shah syndrome277580Graph: Waardenburg-Shah syndromeMouseHumanRatXXXXZfinXXXXX
Wagner syndrome143200Graph: Wagner syndromeMouseHumanRatXXXXXXXXXX
Walker-Warburg syndrome236670Graph: Walker-Warburg syndromeMouseHumanXXXXXXXXXXX
Warfarin resistance122700Graph: Warfarin resistanceMouseHumanRatXXXXXXXXXX
Warfarin sensitivity122700Graph: Warfarin sensitivityMouseHumanRatXXXXXXXXXX
Watson syndrome193520Graph: Watson syndromeMouseHumanXXXXXXXXXXX
Weaver syndrome277590Graph: Weaver syndromeMouseHumanXWormXXXXXXXXX
Weill-Marchesani syndrome, dominant608328Graph: Weill-Marchesani syndrome, dominantMouseHumanXWormXXXXXXXXX
Weissenbacher-Zweymuller syndrome277610Graph: Weissenbacher-Zweymuller syndromeXXXXXXXXXXXXX
Werner syndrome277700Graph: Werner syndromeMouseHumanXXXXXXXXXXX
Weyers acrodental dysostosis193530Graph: Weyers acrodental dysostosisXHumanXXXXXXXXXXX
White sponge nevus193900Graph: White sponge nevusMouseHumanXXXXXXXXXXX
Williams-Beuren syndrome194050Graph: Williams-Beuren syndromeMouseHumanRatXXXXXXXXXX
Wilms tumor194070Graph: Wilms tumorMouseHumanRatXXXXZfinXXXXX
Wilms tumor, somatic194070Graph: Wilms tumor, somaticMouseHumanRatXXXXZfinXXXXX
Wilms tumor, type 1194070Graph: Wilms tumor, type 1MouseHumanRatXXXXZfinXXXXX
Wilson disease277900Graph: Wilson diseaseXHumanRatWormXXXXXXYeastXX
Winchester syndrome277950Graph: Winchester syndromeXHumanRatXXXXXXXXXX
Wiskott-Aldrich syndrome301000Graph: Wiskott-Aldrich syndromeMouseHumanXXXDictyXXXXYeastXX
Witkop syndrome189500Graph: Witkop syndromeMouseHumanXWormXXXXXXXXX
Wolcott-Rallison syndrome226980Graph: Wolcott-Rallison syndromeMouseXRatXXXXXXXXXX
Wolff-Parkinson-White syndrome194200Graph: Wolff-Parkinson-White syndromeMouseXXXXXXXXXYeastXX
Wolfram syndrome222300Graph: Wolfram syndromeXHumanXXXXXXXXXXX

X
OMIM disorder(s)OMIM_idComparisonGraphMouseHumanRatWormFlyDictyChickenZfinRiceTairYeastPombePfalc
XLA and isolated growth hormone deficiency307200Graph: XLA and isolated growth hormone deficiencyMouseHumanXXXXXXXXXXX
Xanthinuria, type I278300Graph: Xanthinuria, type IMouseHumanRatXXXXXXXXXX
Xeroderma pigmentosum, group D278730Graph: Xeroderma pigmentosum, group DMouseHumanXXXXXXXXYeastXX
Xeroderma pigmentosum, group E, DDB-negative subtype278740Graph: Xeroderma pigmentosum, group E, DDB-negative subtypeMouseHumanXXXXXXXXXXX
Xeroderma pigmentosum, group F278760Graph: Xeroderma pigmentosum, group FXHumanXXXXXXXXYeastXX
Xeroderma pigmentosum, group G278780Graph: Xeroderma pigmentosum, group GMouseHumanXXXXXXXXYeastXX
Xeroderma pigmentosum, variant type278750Graph: Xeroderma pigmentosum, variant typeMouseHumanXXXXXXXXYeastXX
Xp11.3 deletion syndrome300578Graph: Xp11.3 deletion syndromeXHumanXXXXXXXXXXX

Y
OMIM disorder(s)OMIM_idComparisonGraphMouseHumanRatWormFlyDictyChickenZfinRiceTairYeastPombePfalc
Yellow nail syndrome153300Graph: Yellow nail syndromeMouseHumanRatXXXXXXXXXX
Yemenite deaf-blind hypopigmentation syndrome601706Graph: Yemenite deaf-blind hypopigmentation syndromeMouseHumanRatXXXXZfinXXXXX

Z
OMIM disorder(s)OMIM_idComparisonGraphMouseHumanRatWormFlyDictyChickenZfinRiceTairYeastPombePfalc
Zellweger syndrome214100Graph: Zellweger syndromeMouseHumanRatWormXXXXXXYeastXX
Zellweger syndrome, complementation group G214100Graph: Zellweger syndrome, complementation group GMouseHumanRatWormXXXXXXYeastXX
Zellweger syndrome-1214100Graph: Zellweger syndrome-1MouseHumanRatWormXXXXXXYeastXX
Zlotogora-Ogur syndrome225000Graph: Zlotogora-Ogur syndromeMouseHumanXXXXXXXXXXX

2
OMIM disorder(s)OMIM_idComparisonGraphMouseHumanRatWormFlyDictyChickenZfinRiceTairYeastPombePfalc
2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency300438Graph: 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiencyMouseHumanRatWormXXXXXXXXX

3
OMIM disorder(s)OMIM_idComparisonGraphMouseHumanRatWormFlyDictyChickenZfinRiceTairYeastPombePfalc
3-methylglutaconic aciduria, type I250950Graph: 3-methylglutaconic aciduria, type IMouseHumanXXXXXXXXXXX
3-methylglutaconicaciduria, type III258501Graph: 3-methylglutaconicaciduria, type IIIXXXXXXXXXXXXX
!Project_name: GO Annotation @ EBI (GOA)
!GOA Human 57.0
!GOC Validation Date: 12/05/2007 $
!Submission Date: 12/5/2007

!Project_name: Mouse Genome Informatics (MGI)
!software version: $Revision: 1.38 $
!date: 12/06/2007 $

!Project_name: Rat Genome Database (RGD)
!CVS Version: Revision: 1.90 $
!GOC Validation Date: 12/01/2007 $
!Submission Date: 7/14/2007

!Project_name: WormBase
!CVS Version: Revision: 1.102 $
!GOC Validation Date: 12/01/2007 $
!Submission Date: 11/26/2007

!Project_name: FlyBase
!CVS Version: Revision: 1.112 $
!GOC Validation Date: 12/01/2007 $
!Submission Date: 11/2/2007

!Project_name: dictyBase
!CVS Version: Revision: 1.147 $
!GOC Validation Date: 12/02/2007 $
!Submission Date: 12/2/2007

!Project_name: GO Annotation @ EBI (GOA)
!GOA Chicken 30.0
!CVS Version: Revision: 1.47 $
!GOC Validation Date: 12/05/2007 $
!Submission Date: 12/5/2007

!Project_name: The Zebrafish Information Network
!CVS Version: Revision: 1.193 $
!GOC Validation Date: 12/04/2007 $
!Submission Date: 12/4/2007

!Project_name: The Arabidopsis Information Resource (TAIR)
!CVS Version: Revision: 1.1182 $
!GOC Validation Date: 12/01/2007 $
!Submission Date: 12/1/2007

!Project_name: Gramene
!CVS Version: Revision: 1.42 $
!GOC Validation Date: 11/24/2007 $
!Submission Date: 9/19/2007

!Project_name: Saccharomyces Genome Database (SGD)
!CVS Version: Revision: 1.1369 $
!GOC Validation Date: 12/01/2007 $
!Submission Date: 11/30/2007

!Project_name: Schizosaccharomyces pombe GeneDB
!CVS Version: Revision: 1.84 $
!GOC Validation Date: 12/03/2007 $
!Submission Date: 12/3/2007

!Project_name: Plasmodium falciparum GeneDB
!CVS Version: Revision: 1.45 $
!GOC Validation Date: 11/26/2007 $
!Submission Date: 11/26/2007