| OMIM ID |
Human Disease |
| 100050 |
Aarskog Syndrome |
| 147800 |
Aase-Smith Syndrome I |
| 600501 |
ABCD Syndrome |
| 100100 |
Abdominal Muscles, Absence of, with Urinary Tract Abnormality and Cryptorchidism |
| 605552 |
Abdominal Obesity-Metabolic Syndrome (3 mouse models) |
| 605572 |
Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 |
| 100200 |
Abducens Palsy |
| 200100 |
Abetalipoproteinemia; ABL (2 mouse models) |
| 300262 |
Abidi X-Linked Mental Retardation Syndrome |
| 200110 |
Ablepharon-Macrostomia Syndrome |
| 200130 |
Absent Eyebrows and Eyelashes with Mental Retardation |
| 100600 |
Acanthosis Nigricans |
| 200170 |
Acanthosis Nigricans with Muscle Cramps and Acral Enlargement |
| 604290 |
Aceruloplasminemia (3 mouse models) |
| 142700 |
Acetabular Dysplasia |
| 100675 |
Acetaminophen Metabolism |
| 200300 |
Acetophenetidin Sensitivity |
| 100678 |
Acetyl-CoA Acetyltransferase 2; ACAT2 |
| 200350 |
Acetyl-CoA Carboxylase-Alpha; ACACA |
| 243400 |
Acetylation, Slow |
| 100680 |
Acetylcholinesterase Expression; ACEE |
| 100740 |
Acetylcholinesterase; ACHE |
| 200400 |
Achalasia, Familial Esophageal (2 mouse models) |
| 231550 |
Achalasia-Addisonianism-Alacrima Syndrome; AAA |
| 200450 |
Achalasia-Microcephaly Syndrome |
| 100700 |
Achard Syndrome |
| 200500 |
Acheiropody (1 mouse model) |
| 200600 |
Achondrogenesis, Type IA; ACG1A |
| 600972 |
Achondrogenesis, Type IB; ACG1B |
| 200610 |
Achondrogenesis, Type II; ACG2 (1 mouse model) |
| 200900 |
Achondroplasia, So-Called, and Severe Combined Immunodeficiency |
| 100800 |
Achondroplasia; ACH (11 mouse models) |
| 100820 |
ACHOO Syndrome |
| 216900 |
Achromatopsia 2; ACHM2 (1 mouse model) |
| 262300 |
Achromatopsia 3; ACHM3 |
| 200950 |
Acid Phosphatase Deficiency |
| 200970 |
Ackerman Syndrome |
| 142690 |
Acne Inversa, Familial |
| 604324 |
Acne, Adult |
| 200990 |
Acrocallosal Syndrome; ACLS |
| 607778 |
Acrocapitofemoral Dysplasia; ACFD |
| 200995 |
Acrocephalopolydactylous Dysplasia |
| 101120 |
Acrocephalopolysyndactyly Type III |
| 201020 |
Acrocephalopolysyndactyly Type IV |
| 201050 |
Acrocraniofacial Dysostosis |
| 201100 |
Acrodermatitis Enteropathica, Zinc-Deficiency Type; AEZ (1 mouse model) |
| 101800 |
Acrodysostosis |
| 603740 |
Acrodysplasia with Ossification Abnormalities, Short Stature, and Fibular Hypoplasia |
| 154400 |
Acrofacial Dysostosis 1, Nager Type; AFD1 |
| 201170 |
Acrofacial Dysostosis Syndrome of Rodriguez |
| 101805 |
Acrofacial Dysostosis, Catania Type |
| 601829 |
Acrofacial Dysostosis, Palagonia Type |
| 201180 |
Acrofrontofacionasal Dysostosis 1 |
| 239710 |
Acrofrontofacionasal Dysostosis 2 |
| 201200 |
Acrogeria, Gottron Type |
| 101840 |
Acrokeratoderma, Hereditary Papulotranslucent |
| 101900 |
Acrokeratosis Verruciformis; AKV |
| 102000 |
Acroleukopathy, Symmetric |
| 102100 |
Acromegaloid Changes, Cutis Verticis Gyrata, and Corneal Leukoma |
| 102150 |
Acromegaloid Facial Appearance Syndrome |
| 606049 |
Acromegaloid Features, Overgrowth, Cleft Palate, and Hernia |
| 603671 |
Acromelic Frontonasal Dysostosis |
| 201250 |
Acromesomelic Dysplasia, Hunter-Thompson Type |
| 602875 |
Acromesomelic Dysplasia, Maroteaux Type; AMDM (1 mouse model) |
| 102350 |
Acromial Dimples |
| 102370 |
Acromicric Dysplasia |
| 102400 |
Acroosteolysis |
| 102500 |
Acroosteolysis with Osteoporosis and Changes in Skull and Mandible |
| 605967 |
Acropectoral Syndrome |
| 102510 |
Acropectorovertebral Dysplasia, F-Form of |
| 102520 |
Acrorenal Syndrome |
| 201310 |
Acrorenal Syndrome, Autosomal Recessive |
| 200980 |
Acrorenal-Mandibular Syndrome |
| 201400 |
Acth Deficiency, Isolated; IAD (1 mouse model) |
| 219080 |
Acth-Independent Macronodular Adrenal Hyperplasia; AIMAH (3 mouse models) |
| 102540 |
Actin, Alpha, Cardiac Muscle; ACTC1 |
| 174770 |
Actinic Prurigo |
| 102574 |
Actinin, Alpha-3; ACTN3 |
| 254900 |
Action Myoclonus-Renal Failure Syndrome; AMRF |
| 602730 |
Activin A Receptor, Type IIB; ACVR2B (1 mouse model) |
| 606752 |
Acute Hemorrhagic Leukoencephalitis |
| 601676 |
Acute Insulin Response |
| 602439 |
Acute Myelogenous Leukemia |
| 612376 |
Acute Promyelocytic Leukemia; APL (1 mouse model) |
| 611126 |
Acyl-Coa Dehydrogenase Family, Member 9, Deficiency of |
| 201460 |
Acyl-CoA Dehydrogenase, Long-Chain, Deficiency of (1 mouse model) |
| 201450 |
Acyl-CoA Dehydrogenase, Medium-Chain, Deficiency of (1 mouse model) |
| 201470 |
Acyl-CoA Dehydrogenase, Short-Chain, Deficiency of (1 mouse model) |
| 201475 |
Acyl-CoA Dehydrogenase, Very Long-Chain, Deficiency of (3 mouse models) |
| 602586 |
Acyl-CoA Thioester Hydrolase, Long-Chain, 1 |
| 102590 |
Acylase, Cobalt-Activated |
| 102650 |
Adactylia, Unilateral |
| 102660 |
Adamantinoma of Long Bones |
| 100300 |
Adams-Oliver Syndrome; AOS |
| 601776 |
Adducted Thumb-Clubfoot Syndrome |
| 201550 |
Adducted Thumbs Syndrome |
| 102600 |
Adenine Phosphoribosyltransferase; APRT (3 mouse models) |
| 102699 |
Adeno-Associated Virus Integration Site 1; AAVS1 |
| 175100 |
Adenomatous Polyposis of the Colon; APC (4 mouse models) |
| 600458 |
Adenomyosis |
| 102710 |
Adenosine Deaminase Complexing Protein 1; ADCP1 |
| 102730 |
Adenosine Deaminase, Elevated, Hemolytic Anemia Due to |
| 102770 |
Adenosine Monophosphate Deaminase 1; AMPD1 |
| 102800 |
Adenosine Triphosphatase Deficiency, Anemia Due to |
| 102900 |
Adenosine Triphosphate, Elevated, of Erythrocytes |
| 612631 |
Adenylate Kinase Deficiency, Hemolytic Anemia Due to |
| 103050 |
Adenylosuccinase Deficiency |
| 103100 |
Adie Pupil |
| 612556 |
Adiponectin, Serum Level of, Quantitative Trait Locus 1; ADIPQTL1 |
| 606770 |
Adiponectin, Serum Level of, Quantitative Trait Locus 2; ADIPQTL2 |
| 606771 |
Adiponectin, Serum Level of, Quantitative Trait Locus 3; ADIPQTL3 |
| 612629 |
Adiponectin, Serum Level of, Quantitative Trait Locus 4; ADIPQTL4 |
| 103200 |
Adiposis Dolorosa |
| 110600 |
ADP-Ribosyltransferase 4; ART4 |
| 202110 |
Adrenal Hyperplasia, Congenital, Due to 17-Alpha-Hydroxylase Deficiency |
| 201910 |
Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency |
| 202010 |
Adrenal Hyperplasia, Congenital, Due to Steroid 11-Beta-Hydroxylase Deficiency |
| 202150 |
Adrenal Hypoplasia, Congenital, with Absent Pituitary Luteinizing Hormone |
| 300200 |
Adrenal Hypoplasia, Congenital; AHC (1 mouse model) |
| 202155 |
Adrenal Hypoplasia, Cytomegalic Type |
| 300250 |
Adrenal Unresponsiveness to ACTH |
| 202300 |
Adrenocortical Carcinoma, Hereditary; ADCC |
| 103230 |
Adrenocortical Hypofunction, Chronic Primary Congenital |
| 202355 |
Adrenocortical Unresponsiveness to ACTH with Postreceptor Defect |
| 202370 |
Adrenoleukodystrophy, Autosomal Neonatal Form |
| 300100 |
Adrenoleukodystrophy; ALD (8 mouse models) |
| 300270 |
Adrenomyodystrophy |
| 103285 |
ADULT Syndrome |
| 604348 |
Advanced Sleep-Phase Syndrome, Familial (3 mouse models) |
| 202400 |
Afibrinogenemia, Congenital (1 mouse model) |
| 610483 |
Agammaglobulinemia, Microcephaly, and Severe Dermatitis |
| 601495 |
Agammaglobulinemia, Non-Bruton Type, Autosomal Recessive |
| 300310 |
Agammaglobulinemia, X-Linked, Type 2; AGMX2 |
| 300755 |
Agammaglobulinemia, X-Linked; XLA (6 mouse models) |
| 202550 |
Aganglionosis, Total Intestinal |
| 612448 |
Age-Related Hearing Impairment 1; ARHI1 |
| 612976 |
Age-Related Hearing Impairment 2; ARHI2 |
| 202600 |
Agenesis of Cerebral White Matter |
| 218000 |
Agenesis of the Corpus Callosum with Peripheral Neuropathy; ACCPN (3 mouse models) |
| 202660 |
Agonadism with Multiple Internal Malformations |
| 600908 |
Agonadism, XY, with Mental Retardation, Short Stature, Retarded Bone Age, and Multiple Extragenital Malformations |
| 608688 |
AICAR Transformylase/IMP Cyclohydrolase, Deficiency of |
| 304050 |
Aicardi Syndrome; AIC |
| 225750 |
Aicardi-Goutieres Syndrome 1; AGS1 (1 mouse model) |
| 610181 |
Aicardi-Goutieres Syndrome 2; AGS2 |
| 610329 |
Aicardi-Goutieres Syndrome 3; AGS3 |
| 610333 |
Aicardi-Goutieres Syndrome 4; AGS4 |
| 612952 |
Aicardi-Goutieres Syndrome 5; AGS5 |
| 103400 |
Ainhum |
| 609465 |
Al-Gazali Syndrome |
| 601549 |
Alacrima |
| 103420 |
Alacrima, Congenital |
| 118450 |
Alagille Syndrome 1; ALGS1 (3 mouse models) |
| 610205 |
Alagille Syndrome 2; ALGS2 |
| 300600 |
Aland Island Eye Disease; AIED |
| 612363 |
Alanine Aminotransferase, Plasma Level of, Quantitative Trait Locus 1 |
| 612364 |
Alanine Aminotransferase, Plasma Level of, Quantitative Trait Locus 2 |
| 202900 |
Alaninuria with Microcephaly, Dwarfism, Enamel Hypoplasia, and Diabetes Mellitus |
| 300500 |
Albinism, Ocular, Type I; OA1 (1 mouse model) |
| 300650 |
Albinism, Ocular, with Late-Onset Sensorineural Deafness; OASD |
| 103470 |
Albinism, Ocular, with Sensorineural Deafness (16 mouse models) |
| 203100 |
Albinism, Oculocutaneous, Type IA; OCA1A |
| 606952 |
Albinism, Oculocutaneous, Type IB; OCA1B |
| 203200 |
Albinism, Oculocutaneous, Type II; OCA2 |
| 203290 |
Albinism, Oculocutaneous, Type III; OCA3 |
| 278400 |
Albinism, Rufous Oculocutaneous; ROCA |
| 300700 |
Albinism-Deafness Syndrome; ADFN |
| 203340 |
Albinism-Microcephaly-Digital Anomalies Syndrome |
| 103600 |
Albumin; ALB |
| 103780 |
Alcohol Dependence (1 mouse model) |
| 610251 |
Alcohol Sensitivity, Acute |
| 100650 |
Aldehyde Dehydrogenase 2 Family; ALDH2 |
| 203450 |
Alexander Disease (7 mouse models) |
| 171720 |
Alkaline Phosphatase, Plasma Level of, Quantitative Trait Locus 1 |
| 612367 |
Alkaline Phosphatase, Plasma Level of, Quantitative Trait Locus 2 |
| 612368 |
Alkaline Phosphatase, Plasma Level of, Quantitative Trait Locus 3 |
| 612369 |
Alkaline Phosphatase, Plasma Level of, Quantitative Trait Locus 4 |
| 203500 |
Alkaptonuria (1 mouse model) |
| 300523 |
Allan-Herndon-Dudley Syndrome; AHDS (1 mouse model) |
| 612396 |
Allantoicase; ALLC |
| 103920 |
Allergic Bronchopulmonary Aspergillosis |
| 607154 |
Allergic Rhinitis |
| 104000 |
Alopecia Areata 1 |
| 610753 |
Alopecia Areata 2 |
| 104100 |
Alopecia Congenita with Keratosis Palmoplantaris |
| 608509 |
Alopecia Universalis Congenita, XY Gonadal Dysgenesis, and Laryngomalacia |
| 203655 |
Alopecia Universalis Congenita; ALUNC (4 mouse models) |
| 109200 |
Alopecia, Androgenetic, 1; AGA1 |
| 300710 |
Alopecia, Androgenetic, 2; AGA2 |
| 612421 |
Alopecia, Androgenetic, 3; AGA3 |
| 300042 |
Alopecia, Congenital |
| 104110 |
Alopecia, Familial Focal |
| 612079 |
Alopecia, Neurologic Defects, and Endocrinopathy Syndrome |
| 104130 |
Alopecia, Psychomotor Epilepsy, Pyorrhea, and Mental Subnormality |
| 203550 |
Alopecia-Contractures-Dwarfism Mental Retardation Syndrome |
| 203600 |
Alopecia-Epilepsy-Oligophrenia Syndrome of Moynahan |
| 203650 |
Alopecia-Mental Retardation Syndrome 1 |
| 610422 |
Alopecia-Mental Retardation Syndrome 2 |
| 601217 |
Alopecia-Mental Retardation Syndrome with Convulsions and Hypergonadotropic Hypogonadism |
| 203700 |
Alpers Diffuse Degeneration of Cerebral Gray Matter with Hepatic Cirrhosis |
| 203760 |
Alpha-2-Deficient Collagen Disease |
| 103950 |
Alpha-2-Macroglobulin; A2M |
| 104250 |
Alpha-2c-Adrenergic Receptor; ADRA2C |
| 608810 |
Alpha-B Crystallinopathy |
| 104150 |
Alpha-Fetoprotein; AFP |
| 203740 |
Alpha-Ketoglutarate Dehydrogenase Deficiency |
| 203750 |
Alpha-Methylacetoacetic Aciduria |
| 604489 |
Alpha-Methylacyl-Coa Racemase; AMACR (1 mouse model) |
| 300448 |
Alpha-Thalassemia Myelodysplasia Syndrome; ATMDS (1 mouse model) |
| 141750 |
Alpha-Thalassemia/Mental Retardation Syndrome, Deletion-Type |
| 301040 |
Alpha-Thalassemia/Mental Retardation Syndrome, Nondeletion Type, X-Linked; (3 mouse models) |
| 609889 |
Alpha/Beta T-Cell Lymphopenia with Gamma/Delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity |
| 104200 |
Alport Syndrome, Autosomal Dominant (1 mouse model) |
| 203780 |
Alport Syndrome, Autosomal Recessive (5 mouse models) |
| 300195 |
Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis Chromosomal Region Gene 1; AMMECR1 |
| 301050 |
Alport Syndrome, X-Linked; ATS (2 mouse models) |
| 203800 |
Alstrom Syndrome; ALMS (3 mouse models) |
| 104290 |
Alternating Hemiplegia of Childhood |
| 265380 |
Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins; (1 mouse model) |
| 606243 |
Alveolar Soft-Part Sarcoma; ASPS |
| 609636 |
Alzheimer Disease 10 |
| 609790 |
Alzheimer Disease 11 |
| 611073 |
Alzheimer Disease 12 |
| 611152 |
Alzheimer Disease 13; AD13 |
| 611154 |
Alzheimer Disease 14; AD14 |
| 611155 |
Alzheimer Disease 15; AD15 |
| 300756 |
Alzheimer Disease 16; AD16 |
| 104310 |
Alzheimer Disease 2 |
| 607822 |
Alzheimer Disease 3 (13 mouse models) |
| 606889 |
Alzheimer Disease 4 (4 mouse models) |
| 602096 |
Alzheimer Disease 5 |
| 605526 |
Alzheimer Disease 6 |
| 606187 |
Alzheimer Disease 7 |
| 607116 |
Alzheimer Disease 8 |
| 608907 |
Alzheimer Disease 9 |
| 604154 |
Alzheimer Disease without Neurofibrillary Tangles |
| 605055 |
Alzheimer Disease, Familial Early-Onset, with Coexisting Amyloid and Prion Pathology |
| 502500 |
Alzheimer Disease, Susceptibility to, Mitochondrial |
| 104300 |
Alzheimer Disease; AD (73 mouse models) |
| 104350 |
Amastia, Bilateral, with Ureteral Triplication and Dysmorphism |
| 204110 |
Amaurosis Congenita, Cone-Rod Type, with Congenital Hypertrichosis |
| 604498 |
Amegakaryocytic Thrombocytopenia, Congenital; CAMT (1 mouse model) |
| 104400 |
Amelia and Terminal Transverse Hemimelia |
| 601360 |
Amelia, Autosomal Recessive |
| 204700 |
Amelogenesis Imperfecta, Hypomaturation Type, Iia1; AI2A1 |
| 612529 |
Amelogenesis Imperfecta, Hypomaturation Type, Iia2; AI2A2 (1 mouse model) |
| 104530 |
Amelogenesis Imperfecta, Hypoplastic Type (1 mouse model) |
| 301200 |
Amelogenesis Imperfecta, Hypoplastic/Hypomaturation, X-Linked 1 (1 mouse model) |
| 301201 |
Amelogenesis Imperfecta, Hypoplastic/Hypomaturation, X-Linked 2 |
| 104500 |
Amelogenesis Imperfecta, Type IB; AI1B (4 mouse models) |
| 204650 |
Amelogenesis Imperfecta, Type Ic; AI1C |
| 204690 |
Amelogenesis Imperfecta, Type IG; AI1G |
| 130900 |
Amelogenesis Imperfecta, Type III; AI3 |
| 104510 |
Amelogenesis Imperfecta, Type IV; AI4 |
| 104570 |
Ameloonychohypohidrotic Syndrome |
| 104600 |
Amenorrhea-Galactorrhea Syndrome |
| 204730 |
Amino Aciduria with Mental Deficiency, Dwarfism, Muscular Dystrophy, Osteoporosis, and Acidosis |
| 609924 |
Aminoacylase 1 Deficiency |
| 204750 |
Aminoadipic Aciduria |
| 600325 |
Aminopterin Syndrome Sine Aminopterin |
| 609056 |
Amish Infantile Epilepsy Syndrome |
| 300194 |
AMME Complex |
| 204800 |
Amobarbital, Deficient N-Hydroxylation of |
| 104760 |
Amyloid Beta A4 Precursor Protein; APP |
| 204850 |
Amyloidosis of Gingiva and Conjunctiva, with Mental Retardation |
| 105150 |
Amyloidosis VI |
| 105210 |
Amyloidosis VII |
| 204900 |
Amyloidosis, Cutaneous Bullous |
| 105200 |
Amyloidosis, Familial Visceral |
| 105120 |
Amyloidosis, Finnish Type (2 mouse models) |
| 105250 |
Amyloidosis, Primary Cutaneous |
| 205000 |
Amyotonia Congenita |
| 105300 |
Amyotrophic Dystonic Paraplegia |
| 105400 |
Amyotrophic Lateral Sclerosis 1; ALS1 (22 mouse models) |
| 612069 |
Amyotrophic Lateral Sclerosis 10; ALS10 |
| 612577 |
Amyotrophic Lateral Sclerosis 11; ALS11 |
| 205100 |
Amyotrophic Lateral Sclerosis 2, Juvenile; ALS2 |
| 606640 |
Amyotrophic Lateral Sclerosis 3; ALS3 |
| 602433 |
Amyotrophic Lateral Sclerosis 4, Juvenile; ALS4 |
| 602099 |
Amyotrophic Lateral Sclerosis 5; ALS5 |
| 608030 |
Amyotrophic Lateral Sclerosis 6 |
| 608031 |
Amyotrophic Lateral Sclerosis 7 |
| 608627 |
Amyotrophic Lateral Sclerosis 8; ALS8 |
| 611895 |
Amyotrophic Lateral Sclerosis 9; ALS9 |
| 205250 |
Amyotrophic Lateral Sclerosis with Polyglucosan Bodies |
| 205200 |
Amyotrophic Lateral Sclerosis, Juvenile, with Dementia |
| 105500 |
Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1 |
| 162100 |
Amyotrophy, Hereditary Neuralgic; HNA |
| 602440 |
Amyotrophy, Monomelic |
| 181405 |
Amyotrophy, Neurogenic Scapuloperoneal, New England Type |
| 602553 |
Anal Atresia, Hypospadias, and Penoscrotal Inversion |
| 105580 |
Anal Canal Carcinoma |
| 105563 |
Anal Sphincter Dysplasia; ASDP |
| 105565 |
Anal Sphincter Myopathy, Internal |
| 607095 |
Anauxetic Dysplasia |
| 170390 |
Andersen Cardiodysrhythmic Periodic Paralysis |
| 300274 |
Androgen Insensitivity Syndrome Due to Coactivator Deficiency |
| 300068 |
Androgen Insensitivity Syndrome; AIS (10 mouse models) |
| 312300 |
Androgen Insensitivity, Partial |
| 105570 |
Androstenone, Ability to Smell |
| 205700 |
Anemia, Autoimmune Hemolytic (1 mouse model) |
| 604315 |
Anemia, Congenital Hypoplastic, with Multiple Congenital Anomalies/Mental Retardation Syndrome |
| 224120 |
Anemia, Dyserythropoietic Congenital, Type I |
| 224100 |
Anemia, Dyserythropoietic Congenital, Type II; CDAN2 |
| 105600 |
Anemia, Dyserythropoietic Congenital, Type III; CDAN3 |
| 206100 |
Anemia, Hypochromic Microcytic, with Iron Overload |
| 206300 |
Anemia, Nonspherocytic Hemolytic, Associated with Abnormality of Red Cell Membrane |
| 206400 |
Anemia, Nonspherocytic Hemolytic, Possibly Due to Defect in Porphyrin Metabolism |
| 301310 |
Anemia, Sideroblastic, and Spinocerebellar Ataxia; ASAT |
| 182170 |
Anemia, Sideroblastic, Autosomal Dominant |
| 205950 |
Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive |
| 206000 |
Anemia, Sideroblastic, Pyridoxine-Responsive, Autosomal Recessive |
| 300751 |
Anemia, Sideroblastic, X-Linked; XLSA |
| 206500 |
Anencephaly (5 mouse models) |
| 105805 |
Aneurysm of Interventricular Septum |
| 105800 |
Aneurysm, Intracranial Berry, 1 |
| 612587 |
Aneurysm, Intracranial Berry, 10 |
| 608542 |
Aneurysm, Intracranial Berry, 2 |
| 609122 |
Aneurysm, Intracranial Berry, 3 |
| 610213 |
Aneurysm, Intracranial Berry, 4 |
| 610402 |
Aneurysm, Intracranial Berry, 5 |
| 611892 |
Aneurysm, Intracranial Berry, 6 |
| 612161 |
Aneurysm, Intracranial Berry, 7 |
| 612162 |
Aneurysm, Intracranial Berry, 8 |
| 612586 |
Aneurysm, Intracranial Berry, 9 |
| 606179 |
Aneurysmal Bone Cysts |
| 105835 |
Angel-Shaped Phalangoepiphyseal Dysplasia; ASPED |
| 105830 |
Angelman Syndrome; AS (4 mouse models) |
| 610618 |
Angioedema, Hereditary, Type III; HAE III |
| 106100 |
Angioedema, Hereditary; HAE |
| 607140 |
Angioid Streaks |
| 600419 |
Angiokeratoma Corporis Diffusum with Arteriovenous Fistulas |
| 206550 |
Angiolipomatosis, Familial |
| 106050 |
Angioma Serpiginosum, Autosomal Dominant |
| 300652 |
Angioma Serpiginosum, X-Linked |
| 106070 |
Angioma, Hereditary Neurocutaneous |
| 607859 |
Angioma, Tufted |
| 206570 |
Angiomatosis, Diffuse Corticomeningeal, of Divry and Van Bogaert |
| 611773 |
Angiopathy, Hereditary, with Nephropathy, Aneurysms, and Muscle Cramps; |
| 106180 |
Angiotensin I-Converting Enzyme; ACE |
| 106160 |
Angiotensin II Binding Protein |
| 300034 |
Angiotensin II Receptor, Type 2; AGTR2 |
| 106150 |
Angiotensinogen; AGT |
| 206600 |
Anhidrosis |
| 106190 |
Anhidrosis, Familial Generalized, with Normal Sweat Glands |
| 106220 |
Aniridia and Absent Patella |
| 206700 |
Aniridia, Cerebellar Ataxia, and Mental Deficiency |
| 106230 |
Aniridia, Microcornea, and Spontaneously Reabsorbed Cataract |
| 206750 |
Aniridia, Partial, with Unilateral Renal Agenesis and Psychomotor Retardation |
| 106210 |
Aniridia; AN (11 mouse models) |
| 106240 |
Anisocoria |
| 605746 |
Anisomastia |
| 106250 |
Ankyloblepharon Filiforme Adnatum and Cleft Palate |
| 106260 |
Ankyloblepharon-Ectodermal Defects-Cleft Lip/Palate |
| 106280 |
Ankyloglossia (1 mouse model) |
| 106400 |
Ankylosing Vertebral Hyperostosis with Tylosis |
| 608774 |
Ankyrin Repeat and Kinase Domain Containing 1; ANKK1 |
| 106500 |
Annular Erythema |
| 206780 |
Anodontia of Permanent Dentition |
| 206800 |
Anonychia Congenita (1 mouse model) |
| 106750 |
Anonychia with Flexural Pigmentation |
| 607214 |
Anonychia, Total, with Microcephaly |
| 106900 |
Anonychia-Ectrodactyly |
| 107000 |
Anonychia-Onychodystrophy |
| 106990 |
Anonychia-Onychodystrophy with Brachydactyly Type B and Ectrodactyly |
| 106995 |
Anonychia-Onychodystrophy with Hypoplasia or Absence of Distal Phalanges |
| 107100 |
Anorectal Anomalies (1 mouse model) |
| 606788 |
Anorexia Nervosa, Susceptibility to, 1; ANON1 |
| 301700 |
Anosmia |
| 207000 |
Anosmia for Isobutyric Acid |
| 107200 |
Anosmia, Congenital |
| 601427 |
Anterior Chamber Cleavage Disorder, Cerebellar Hypoplasia, Hypothyroidism, and Tracheal Stenosis |
| 107250 |
Anterior Segment Mesenchymal Dysgenesis; ASMD (6 mouse models) |
| 158020 |
Antigen Defined By Monoclonal Antibody 4f2, Light Chain |
| 158030 |
Antigen Defined By Monoclonal Antibody Aj9 |
| 158040 |
Antigen Defined By Monoclonal Antibody T87 |
| 107320 |
Antiphospholipid Syndrome, Familial |
| 107290 |
Antipyrine Metabolism |
| 604893 |
Antisense IGF2R |
| 107300 |
Antithrombin III Deficiency (1 mouse model) |
| 207300 |
Antithrombin, Familial Hemorrhagic Diathesis Due to |
| 107440 |
Antiviral State Repressor, Regulator Of; AVRR |
| 207410 |
Antley-Bixler Syndrome; ABS |
| 207500 |
Anus, Imperforate |
| 301800 |
Anus, Imperforate |
| 100070 |
Aortic Aneurysm, Familial Abdominal 1 |
| 609782 |
Aortic Aneurysm, Familial Abdominal 2 |
| 611891 |
Aortic Aneurysm, Familial Abdominal 3 |
| 607086 |
Aortic Aneurysm, Familial Thoracic 1; AAT1 |
| 607087 |
Aortic Aneurysm, Familial Thoracic 2; AAT2 |
| 132900 |
Aortic Aneurysm, Familial Thoracic 4; AAT4 |
| 611788 |
Aortic Aneurysm, Familial Thoracic 6; AAT6 |
| 604622 |
Aortic Aneurysm, Giant Congenital |
| 107500 |
Aortic Arch Anomaly with Peculiar Facies and Mental Retardation |
| 107550 |
Aortic Arch Interruption, Facial Palsy, and Retinal Coloboma |
| 109730 |
Aortic Valve Disease (1 mouse model) |
| 101200 |
Apert Syndrome (4 mouse models) |
| 610256 |
Aphakia, Congenital Primary |
| 600384 |
Aphalangia, Partial, with Syndactyly and Duplication of Metatarsal IV |
| 207620 |
Aphalangy with Hemivertebrae |
| 600360 |
Aplasia Cutis Congenita of Limbs, Recessive |
| 600268 |
Aplasia Cutis Congenita with Epibulbar Dermoids |
| 207731 |
Aplasia Cutis Congenita with Intestinal Lymphangiectasia |
| 601075 |
Aplasia Cutis Congenita, High Myopia, and Cone-Rod Dysfunction |
| 107600 |
Aplasia Cutis Congenita, Nonsyndromic; ACC |
| 207740 |
Aplasia of Extensor Muscles of Fingers, Unilateral, with Generalized Polyneuropathy |
| 180920 |
Aplasia of Lacrimal and Salivary Glands; ALSG |
| 609135 |
Aplastic Anemia |
| 107640 |
Apnea, Central Sleep |
| 207720 |
Apnea, Central Sleep |
| 107650 |
Apnea, Obstructive Sleep |
| 107670 |
Apolipoprotein A-Ii; APOA2 |
| 107730 |
Apolipoprotein B; APOB (11 mouse models) |
| 207750 |
Apolipoprotein C-II Deficiency |
| 107720 |
Apolipoprotein C-Iii; APOC3 |
| 107741 |
Apolipoprotein E; APOE (6 mouse models) |
| 107760 |
Apolipoprotein F; APOF |
| 152200 |
Apolipoprotein(a); LPA |
| 207765 |
Apparent Mineralocorticoid Excess, Type 2; AME2 |
| 107700 |
Appendicitis, Proneness to |
| 603119 |
Apraxia of Eyelid Opening |
| 601374 |
Aprosencephaly and Cerebellar Dysgenesis |
| 207770 |
Aprosencephaly Syndrome |
| 602914 |
Aquaporin 9; AQP9 |
| 207790 |
Arachnoid Cysts, Intracranial |
| 107750 |
Arbitrary Restriction Polymorphism 1 |
| 107800 |
Arcus Corneae |
| 207780 |
Aredyld |
| 612718 |
Arginine:glycine Amidinotransferase Deficiency |
| 207800 |
Argininemia (1 mouse model) |
| 207900 |
Argininosuccinic Aciduria (1 mouse model) |
| 603457 |
Arhinia, Choanal Atresia, and Microphthalmia |
| 243910 |
Arima Syndrome |
| 107850 |
Arm Folding Preference |
| 300261 |
Armfield X-Linked Mental Retardation Syndrome |
| 107900 |
Arms, Malformation of |
| 139300 |
Aromatase Excess Syndrome; AEXS (1 mouse model) |
| 107920 |
Aromatic Alpha-Keto Acid Reductase |
| 608643 |
Aromatic L-Amino Acid Decarboxylase Deficiency |
| 107950 |
Arrhenoblastoma--Thyroid Adenoma |
| 107970 |
Arrhythmogenic Right Ventricular Dysplasia, Familial, 1; ARVD1 (1 mouse model) |
| 610193 |
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10; ARVD10 |
| 610476 |
Arrhythmogenic Right Ventricular Dysplasia, Familial, 11; ARVD11 |
| 611528 |
Arrhythmogenic Right Ventricular Dysplasia, Familial, 12; ARVD12 |
| 600996 |
Arrhythmogenic Right Ventricular Dysplasia, Familial, 2; ARVD2 (1 mouse model) |
| 602086 |
Arrhythmogenic Right Ventricular Dysplasia, Familial, 3; ARVD3 |
| 602087 |
Arrhythmogenic Right Ventricular Dysplasia, Familial, 4; ARVD4 |
| 604400 |
Arrhythmogenic Right Ventricular Dysplasia, Familial, 5; ARVD5 |
| 604401 |
Arrhythmogenic Right Ventricular Dysplasia, Familial, 6 |
| 609160 |
Arrhythmogenic Right Ventricular Dysplasia, Familial, 7 (1 mouse model) |
| 607450 |
Arrhythmogenic Right Ventricular Dysplasia, Familial, 8; ARVD8 |
| 609040 |
Arrhythmogenic Right Ventricular Dysplasia, Familial, 9; ARVD9 |
| 208000 |
Arterial Calcification, Generalized, of Infancy; GACI |
| 600459 |
Arterial Dissection with Lentiginosis |
| 602531 |
Arterial Occlusive Disease, Progressive, with Hypertension, Heart Defects, Bone Fragility, and Brachysyndactyly |
| 208050 |
Arterial Tortuosity Syndrome; ATS (1 mouse model) |
| 108000 |
Arteries, Anomalies of |
| 208060 |
Arteriosclerosis, Severe Juvenile |
| 108010 |
Arteriovenous Malformations of the Brain |
| 108050 |
Arteritis, Familial Granulomatous, with Juvenile Polyarthritis |
| 108100 |
Arthritis, Sacroiliac |
| 601701 |
Arthrogryposis and Ectodermal Dysplasia |
| 208155 |
Arthrogryposis Multiplex Congenita with Whistling Face |
| 208100 |
Arthrogryposis Multiplex Congenita, Neurogenic Type; AMCN (1 mouse model) |
| 108110 |
Arthrogryposis Multiplex Congenita; AMC |
| 610001 |
Arthrogryposis Multiplex with Deafness, Inguinal Hernias, and Early Death |
| 208158 |
Arthrogryposis with Hyperkeratosis |
| 108120 |
Arthrogryposis, Distal, Type 1; DA1 |
| 187370 |
Arthrogryposis, Distal, Type 10; DA10 |
| 193700 |
Arthrogryposis, Distal, Type 2A; DA2A |
| 601680 |
Arthrogryposis, Distal, Type 2B; DA2B |
| 121070 |
Arthrogryposis, Distal, Type 2E |
| 609128 |
Arthrogryposis, Distal, Type 4; DA4 |
| 108145 |
Arthrogryposis, Distal, Type 5; DA5 |
| 208080 |
Arthrogryposis, Distal, with Hypopituitarism, Mental Retardation, and Facial Anomalies |
| 208081 |
Arthrogryposis, Distal, with Mental Retardation and Characteristic Facies |
| 301815 |
Arthrogryposis, Ectodermal Dysplasia, Cleft Lip/Palate, and Developmental Delay |
| 208085 |
Arthrogryposis, Renal Dysfunction, and Cholestasis |
| 300158 |
Arthrogryposis, X-Linked, Type V; AMCX5 |
| 208200 |
Arthrogryposis-Like Disorder |
| 108200 |
Arthrogryposis-Like Hand Anomaly and Sensorineural Deafness |
| 605935 |
Arthropathy, Erosive |
| 208230 |
Arthropathy, Progressive Pseudorheumatoid, of Childhood; PPAC |
| 611618 |
Arthropathy, Tendinous Calcinosis, and Progeroid Features |
| 108320 |
Artichoke, Modification of Taste By |
| 301835 |
Arts Syndrome; ARTS |
| 108340 |
Aryl Hydrocarbon Hydroxylase Inducibility |
| 600950 |
Arylalkylamine N-Acetyltransferase; AANAT |
| 604392 |
Arylhydrocarbon-Interacting Receptor Protein-Like 1; AIPL1 |
| 604291 |
Ascaris Lumbricoides Infection, Susceptibility to |
| 208300 |
Ascites, Chylous |
| 108390 |
Asparagus, Specific Smell Hypersensitivity |
| 208400 |
Aspartylglucosaminuria (2 mouse models) |
| 608638 |
Asperger Syndrome, Susceptibility to, 1 |
| 608631 |
Asperger Syndrome, Susceptibility to, 2 |
| 608781 |
Asperger Syndrome, Susceptibility to, 3 |
| 609954 |
Asperger Syndrome, Susceptibility to, 4 |
| 300494 |
Asperger Syndrome, X-Linked, Susceptibility to, 1 |
| 300497 |
Asperger Syndrome, X-Linked, Susceptibility to, 2 |
| 108420 |
Aspermiogenesis Factor |
| 208500 |
Asphyxiating Thoracic Dystrophy 1; ATD1 (2 mouse models) |
| 611263 |
Asphyxiating Thoracic Dystrophy 2; ATD2 |
| 613091 |
Asphyxiating Thoracic Dystrophy 3; ATD3 |
| 608223 |
Aspirin Resistance |
| 208530 |
Asplenia with Cardiovascular Anomalies (3 mouse models) |
| 208550 |
Asthma, Nasal Polyps, and Aspirin Intolerance |
| 208600 |
Asthma, Short Stature, and Elevated Iga |
| 600807 |
Asthma, Susceptibility to (6 mouse models) |
| 607277 |
Asthma-Related Traits, Susceptibility to, 1 |
| 608584 |
Asthma-Related Traits, Susceptibility to, 2 |
| 609958 |
Asthma-Related Traits, Susceptibility to, 3 |
| 610906 |
Asthma-Related Traits, Susceptibility to, 4 |
| 611064 |
Asthma-Related Traits, Susceptibility to, 5 |
| 611403 |
Asthma-Related Traits, Susceptibility to, 6 |
| 611960 |
Asthma-Related Traits, Susceptibility to, 7; ASRT7 |
| 603047 |
Astigmatism |
| 108450 |
Asymmetric Short Stature Syndrome |
| 108700 |
Ataxia with Fasciculations |
| 208700 |
Ataxia with Myoclonic Epilepsy and Presenile Dementia |
| 208750 |
Ataxia, Deafness, and Cardiomyopathy |
| 208920 |
Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia; |
| 608984 |
Ataxia, Sensory, Autosomal Dominant |
| 108600 |
Ataxia, Spastic, 1, Autosomal Dominant; SPAX1 |
| 611302 |
Ataxia, Spastic, 2, Autosomal Recessive; SPAX2 |
| 611390 |
Ataxia, Spastic, 3, Autosomal Recessive; SPAX3 |
| 108650 |
Ataxia, Spastic, with Congenital Miosis |
| 208850 |
Ataxia-Deafness-Retardation Syndrome |
| 208870 |
Ataxia-Microcephaly-Cataract Syndrome |
| 208910 |
Ataxia-Telangiectasia with Generalized Skin Pigmentation and Early Death |
| 604391 |
Ataxia-Telangiectasia-Like Disorder; ATLD |
| 208900 |
Ataxia-Telangiectasia; AT (6 mouse models) |
| 209000 |
Ataxic Diplegia with Defective Cellular Immunity |
| 108720 |
Atelosteogenesis, Type I; AOI |
| 256050 |
Atelosteogenesis, Type II; AOII |
| 108721 |
Atelosteogenesis, Type III; AOIII |
| 601536 |
Athabaskan Brainstem Dysgenesis Syndrome; ABDS |
| 108725 |
Atherosclerosis Susceptibility; ATHS |
| 209010 |
Atherosclerosis, Premature, with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease |
| 209050 |
Athrombia, Essential |
| 300431 |
Atkin-Flaitz Syndrome |
| 209100 |
Atonic-Astatic Syndrome of Foerster |
| 516060 |
Atp Synthase 6; MTATP6 |
| 516070 |
Atp Synthase 8; MTATP8 |
| 600046 |
ATP-Binding Cassette, Subfamily A, Member 1; ABCA1 |
| 170995 |
ATP-Binding Cassette, Subfamily D, Member 3; ABCD3 |
| 209300 |
Atransferrinemia (2 mouse models) |
| 108760 |
Atresia of External Auditory Canal and Conduction Deafness |
| 608583 |
Atrial Fibrillation, Familial, 1; ATFB1 |
| 608988 |
Atrial Fibrillation, Familial, 2; ATFB2 |
| 607554 |
Atrial Fibrillation, Familial, 3; ATFB3 |
| 611493 |
Atrial Fibrillation, Familial, 4; ATFB4 |
| 611494 |
Atrial Fibrillation, Familial, 5; ATFB5 |
| 612201 |
Atrial Fibrillation, Familial, 6; ATFB6 |
| 612240 |
Atrial Fibrillation, Familial, 7; ATFB7 |
| 613055 |
Atrial Fibrillation, Familial, 8; ATFB8 |
| 108800 |
Atrial Septal Defect 1; ASD1 (2 mouse models) |
| 607941 |
Atrial Septal Defect 2; ASD2 |
| 611363 |
Atrial Septal Defect 4; ASD4 |
| 612794 |
Atrial Septal Defect 5; ASD5 |
| 613087 |
Atrial Septal Defect 6; ASD6 |
| 108900 |
Atrial Septal Defect with Atrioventricular Conduction Defects (2 mouse models) |
| 603642 |
Atrial Septal Defect, Secundum, with Various Cardiac and Noncardiac Defects |
| 108770 |
Atrial Standstill |
| 108950 |
Atrial Tachyarrhythmia with Short PR Interval |
| 209500 |
Atrichia with Papular Lesions; APL (4 mouse models) |
| 108970 |
Atriopeptidase |
| 108980 |
Atrioventricular Conduction Time |
| 209600 |
Atrioventricular Dissociation |
| 600123 |
Atrioventricular Septal Defect with Blepharophimosis and Anal and Radial Defects |
| 606215 |
Atrioventricular Septal Defect, Susceptibility to, 1; AVSD1 |
| 606217 |
Atrioventricular Septal Defect, Susceptibility to, 2; AVSD2 |
| 600309 |
Atrioventricular Septal Defect; AVSD (2 mouse models) |
| 601341 |
Atrophia Maculosa Varioliformis Cutis, Familial; AMVC |
| 209700 |
Atrophodermia Vermiculata |
| 608903 |
Attention Deficit-Hyperactivity Disorder, Susceptibility to, 1 |
| 608904 |
Attention Deficit-Hyperactivity Disorder, Susceptibility to, 2 |
| 608905 |
Attention Deficit-Hyperactivity Disorder, Susceptibility to, 3 |
| 608906 |
Attention Deficit-Hyperactivity Disorder, Susceptibility to, 4 |
| 612311 |
Attention Deficit-Hyperactivity Disorder, Susceptibility to, 5 |
| 612312 |
Attention Deficit-Hyperactivity Disorder, Susceptibility to, 6 |
| 613003 |
Attention Deficit-Hyperactivity Disorder, Susceptibility to, 7 |
| 143465 |
Attention Deficit-Hyperactivity Disorder; ADHD (2 mouse models) |
| 209950 |
Atypical Mycobacteriosis, Familial |
| 300636 |
Atypical Mycobacteriosis, Familial, X-Linked 1; AMCBX1 |
| 300645 |
Atypical Mycobacteriosis, Familial, X-Linked 2 |
| 609129 |
Auditory Neuropathy, Autosomal Dominant, 1; AUNA1 |
| 607842 |
Aural Atresia, Congenital |
| 209770 |
Aural Atresia, Multiple Congenital Anomalies, and Mental Retardation |
| 602483 |
Auriculocondylar Syndrome |
| 109000 |
Auriculoosteodysplasia |
| 109050 |
Aurocephalosyndactyly |
| 209800 |
Australia Antigen |
| 209850 |
Autism (2 mouse models) |
| 611016 |
Autism, Susceptibility to, 10; AUTS10 |
| 610836 |
Autism, Susceptibility to, 11; AUTS11 |
| 610838 |
Autism, Susceptibility to, 12; AUTS12 |
| 610908 |
Autism, Susceptibility to, 13; AUTS13 |
| 611913 |
Autism, Susceptibility to, 14; AUTS14 |
| 612100 |
Autism, Susceptibility to, 15; AUTS15 |
| 608049 |
Autism, Susceptibility to, 3 |
| 606053 |
Autism, Susceptibility to, 5; AUTS5 |
| 609378 |
Autism, Susceptibility to, 6; AUTS6 |
| 610676 |
Autism, Susceptibility to, 7; AUTS7 |
| 607373 |
Autism, Susceptibility to, 8; AUTS8 |
| 611015 |
Autism, Susceptibility to, 9; AUTS9 (1 mouse model) |
| 300425 |
Autism, X-Linked, Susceptibility to, 1 Autsx1 (1 mouse model) |
| 300495 |
Autism, X-Linked, Susceptibility to, 2 |
| 300496 |
Autism, X-Linked, Susceptibility to, 3 |
| 109100 |
Autoimmune Disease (2 mouse models) |
| 607836 |
Autoimmune Disease, Susceptibility to, 1; AIS1 |
| 608391 |
Autoimmune Disease, Susceptibility to, 2; AIS2 |
| 608392 |
Autoimmune Disease, Susceptibility to, 3; AIS3 |
| 609400 |
Autoimmune Disease, Susceptibility to, 4; AIS4 |
| 603909 |
Autoimmune Lymphoproliferative Syndrome, Type IIA; ALPS2A |
| 601859 |
Autoimmune Lymphoproliferative Syndrome; ALPS (4 mouse models) |
| 240300 |
Autoimmune Polyendocrine Syndrome, Type I; APS1 (9 mouse models) |
| 269200 |
Autoimmune Polyendocrine Syndrome, Type II; APS2 |
| 608173 |
Autoimmune Thyroid Disease, Susceptibility to, 1 |
| 608174 |
Autoimmune Thyroid Disease, Susceptibility to, 2 |
| 608175 |
Autoimmune Thyroid Disease, Susceptibility to, 3; AITD3 |
| 608176 |
Autoimmune Thyroid Disease, Susceptibility to, 4 |
| 209880 |
Autonomic Control, Congenital Failure of (2 mouse models) |
| 608805 |
Avascular Necrosis of Femoral Head, Primary |
| 109120 |
Axenfeld-Rieger Anomaly with Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, and Skeletal Abnormalities |
| 180500 |
Axenfeld-Rieger Syndrome, Type 1; RIEG1 (8 mouse models) |
| 601499 |
Axenfeld-Rieger Syndrome, Type 2; RIEG2 |
| 602482 |
Axenfeld-Rieger Syndrome, Type 3; RIEG3 (1 mouse model) |
| 109130 |
Axial Osteomalacia |
| 270960 |
Azoospermia Due to Perturbations of Meiosis (1 mouse model) |
| 606766 |
Azoospermia, Nonobstructive |
| 109160 |
Azotemia, Familial |
