| OMIM ID |
Human Disease |
| 305400 |
Aarskog-Scott Syndrome; AAS |
| 100050 |
Aarskog Syndrome, Autosomal Dominant |
| 147800 |
Aase-Smith Syndrome I |
| 600501 |
Abcd Syndrome; ABCDS |
| 100100 |
Abdominal Muscles, Absence of, with Urinary Tract Abnormality and Cryptorchidism |
| 605552 |
Abdominal Obesity-Metabolic Syndrome (8 mouse models) |
| 100200 |
Abducens Palsy |
| 200100 |
Abetalipoproteinemia; ABL |
| 300262 |
Abidi X-Linked Mental Retardation Syndrome; MRXSAB |
| 200110 |
Ablepharon-Macrostomia Syndrome |
| 200130 |
Absent Eyebrows and Eyelashes with Mental Retardation |
| 100600 |
Acanthosis Nigricans |
| 200170 |
Acanthosis Nigricans with Muscle Cramps and Acral Enlargement |
| 614097 |
Acatalasemia |
| 614401 |
Accelerated Tumor Formation, Susceptibility To; ACTFS |
| 604290 |
Aceruloplasminemia (3 mouse models) |
| 142700 |
Acetabular Dysplasia |
| 100675 |
Acetaminophen Metabolism |
| 200300 |
Acetophenetidin Sensitivity |
| 243400 |
Acetylation, Slow |
| 614055 |
Acetyl-Coa Acetyltransferase-2 Deficiency; ACAT2D |
| 613933 |
Acetyl-Coa Carboxylase Deficiency; ACACAD |
| 231550 |
Achalasia-Addisonianism-Alacrima Syndrome; AAAS |
| 200400 |
Achalasia, Familial Esophageal (2 mouse models) |
| 200450 |
Achalasia-Microcephaly Syndrome |
| 100700 |
Achard Syndrome |
| 200500 |
Acheiropody (1 mouse model) |
| 200600 |
Achondrogenesis, Type IA; ACG1A (1 mouse model) |
| 600972 |
Achondrogenesis, Type IB; ACG1B |
| 200610 |
Achondrogenesis, Type II; ACG2 (1 mouse model) |
| 100800 |
Achondroplasia; ACH (12 mouse models) |
| 100820 |
ACHOO Syndrome |
| 216900 |
Achromatopsia 2; ACHM2 (1 mouse model) |
| 262300 |
Achromatopsia 3; ACHM3 |
| 613856 |
Achromatopsia 4; ACHM4 (1 mouse model) |
| 200950 |
Acid Phosphatase Deficiency |
| 200970 |
Ackerman Syndrome |
| 604324 |
Acne, Adult |
| 142690 |
Acne Inversa, Familial, 1; ACNINV1 |
| 613736 |
Acne Inversa, Familial, 2; ACNINV2 |
| 613737 |
Acne Inversa, Familial, 3; ACNINV3 |
| 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 1, with or without Hormone Resistance; ACRDYS1 |
| 614613 |
Acrodysostosis 2, with or without Hormone Resistance; ACRDYS2 |
| 603740 |
Acrodysplasia with Ossification Abnormalities, Short Stature, and Fibular Hypoplasia |
| 154400 |
Acrofacial Dysostosis 1, Nager Type; AFD1 |
| 101805 |
Acrofacial Dysostosis, Catania Type |
| 601829 |
Acrofacial Dysostosis, Palagonia Type |
| 201170 |
Acrofacial Dysostosis Syndrome of Rodriguez |
| 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 (2 mouse models) |
| 102350 |
Acromial Dimples |
| 102370 |
Acromicric Dysplasia; ACMICD |
| 102400 |
Acroosteolysis |
| 605967 |
Acropectoral Syndrome; ACRPS |
| 102510 |
Acropectorovertebral Dysplasia; ACRPV |
| 200980 |
Acrorenal-Mandibular Syndrome |
| 102520 |
Acrorenal Syndrome |
| 201310 |
Acrorenal Syndrome, Autosomal Recessive |
| 201400 |
Acth Deficiency, Isolated; IAD (1 mouse model) |
| 219080 |
Acth-Independent Macronodular Adrenal Hyperplasia; AIMAH (2 mouse models) |
| 174770 |
Actinic Prurigo |
| 603416 |
Activator of Liver Function 1; ALFN1 |
| 606752 |
Acute Hemorrhagic Leukoencephalitis |
| 601676 |
Acute Insulin Response |
| 602439 |
Acute Myelogenous Leukemia |
| 612376 |
Acute Promyelocytic Leukemia; APL (2 mouse models) |
| 102590 |
Acylase, Cobalt-Activated |
| 611126 |
Acyl-Coa Dehydrogenase Family, Member 9, Deficiency of |
| 201450 |
Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency Of; ACADMD (1 mouse model) |
| 201470 |
Acyl-Coa Dehydrogenase, Short-Chain, Deficiency Of; ACADSD (1 mouse model) |
| 201475 |
Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency Of; ACADVLD (4 mouse models) |
| 602586 |
Acyl-CoA Thioester Hydrolase, Long-Chain, 1 |
| 102650 |
Adactylia, Unilateral |
| 102660 |
Adamantinoma of Long Bones |
| 100300 |
Adams-Oliver Syndrome 1; AOS1 |
| 614219 |
Adams-Oliver Syndrome 2; AOS2 |
| 614814 |
Adams-Oliver Syndrome 3; AOS3 |
| 201550 |
Adducted Thumbs Syndrome |
| 614723 |
Adenine Phosphoribosyltransferase Deficiency; APRTD (3 mouse models) |
| 600458 |
Adenomyosis |
| 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 |
| 136000 |
Adermatoglyphia; ADERM |
| 129200 |
Adermatoglyphia with Congenital Facial Milia and Acral Blisters, Digital Contractures, and Nail Abnormalities |
| 103100 |
Adie Pupil |
| 103200 |
Adiposis Dolorosa |
| 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 |
| 300200 |
Adrenal Hypoplasia, Congenital; AHC (1 mouse model) |
| 202150 |
Adrenal Hypoplasia, Congenital, with Absent Pituitary Luteinizing Hormone |
| 202155 |
Adrenal Hypoplasia, Cytomegalic Type |
| 613743 |
Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete |
| 202300 |
Adrenocortical Carcinoma, Hereditary; ADCC |
| 103230 |
Adrenocortical Hypofunction, Chronic Primary Congenital |
| 202355 |
Adrenocortical Unresponsiveness to ACTH with Postreceptor Defect |
| 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) |
| 601495 |
Agammaglobulinemia 1, Autosomal Recessive; AGM1 |
| 613500 |
Agammaglobulinemia 2, Autosomal Recessive; AGM2 |
| 613501 |
Agammaglobulinemia 3, Autosomal Recessive; AGM3 |
| 613502 |
Agammaglobulinemia 4, Autosomal Recessive; AGM4 |
| 613506 |
Agammaglobulinemia 5, Autosomal Dominant; AGM5 |
| 612692 |
Agammaglobulinemia 6, Autosomal Recessive; AGM6 |
| 610483 |
Agammaglobulinemia, Microcephaly, and Severe Dermatitis |
| 300310 |
Agammaglobulinemia, X-Linked, Type 2; AGMX2 |
| 300755 |
Agammaglobulinemia, X-Linked; XLA (10 mouse models) |
| 202550 |
Aganglionosis, Total Intestinal |
| 202600 |
Agenesis of Cerebral White Matter |
| 613623 |
Agenesis of the Corpus Callosum and Congenital Lymphedema |
| 218000 |
Agenesis of the Corpus Callosum with Peripheral Neuropathy; ACCPN (3 mouse models) |
| 612448 |
Age-Related Hearing Impairment 1; ARHI1 |
| 612976 |
Age-Related Hearing Impairment 2; ARHI2 |
| 202650 |
Agnathia-Otocephaly Complex; AGOTC |
| 600908 |
Agonadism, 46,xy, with Mental Retardation, Short Stature, Retarded Bone Age, and Multiple Extragenital Malformations |
| 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 |
| 615010 |
Aicardi-Goutieres Syndrome 6; AGS6 |
| 304050 |
Aicardi Syndrome; AIC |
| 608688 |
Aicar Transformylase/Imp Cyclohydrolase Deficiency |
| 103400 |
Ainhum |
| 103420 |
Alacrima, Congenital |
| 601549 |
Alacrima, Congenital |
| 118450 |
Alagille Syndrome 1; ALGS1 (5 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 |
| 614687 |
Alar Cleft, Isolated |
| 615071 |
Alazami Syndrome; ALAZS |
| 300700 |
Albinism-Deafness Syndrome; ADFN |
| 203340 |
Albinism-Microcephaly-Digital Anomalies Syndrome |
| 300500 |
Albinism, Ocular, Type I; OA1 (1 mouse model) |
| 300650 |
Albinism, Ocular, with Late-Onset Sensorineural Deafness; OASD |
| 103470 |
Albinism, Ocular, with Sensorineural Deafness (14 mouse models) |
| 203100 |
Albinism, Oculocutaneous, Type IA; OCA1A (1 mouse model) |
| 606952 |
Albinism, Oculocutaneous, Type IB; OCA1B (1 mouse model) |
| 203290 |
Albinism, Oculocutaneous, Type III; OCA3 |
| 203200 |
Albinism, Oculocutaneous, Type II; OCA2 |
| 606574 |
Albinism, Oculocutaneous, Type IV; OCA4 (7 mouse models) |
| 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) |
| 609465 |
Al-Gazali Syndrome |
| 203500 |
Alkaptonuria (1 mouse model) |
| 300523 |
Allan-Herndon-Dudley Syndrome; AHDS (1 mouse model) |
| 103920 |
Allergic Bronchopulmonary Aspergillosis, Familial |
| 607154 |
Allergic Rhinitis |
| 109200 |
Alopecia, Androgenetic, 1; AGA1 |
| 300710 |
Alopecia, Androgenetic, 2; AGA2 |
| 612421 |
Alopecia, Androgenetic, 3; AGA3 |
| 104000 |
Alopecia Areata 1 |
| 610753 |
Alopecia Areata 2 |
| 300042 |
Alopecia, Congenital |
| 203550 |
Alopecia-Contractures-Dwarfism Mental Retardation Syndrome |
| 203600 |
Alopecia-Epilepsy-Oligophrenia Syndrome of Moynahan |
| 104110 |
Alopecia, Familial Focal |
| 203650 |
Alopecia-Mental Retardation Syndrome 1; APMR1 |
| 610422 |
Alopecia-Mental Retardation Syndrome 2; APMR2 |
| 613930 |
Alopecia-Mental Retardation Syndrome 3; APMR3 |
| 601217 |
Alopecia-Mental Retardation Syndrome with Convulsions and Hypergonadotropic Hypogonadism |
| 612079 |
Alopecia, Neurologic Defects, and Endocrinopathy Syndrome |
| 104130 |
Alopecia, Psychomotor Epilepsy, Pyorrhea, and Mental Subnormality |
| 203655 |
Alopecia Universalis Congenita; ALUNC (3 mouse models) |
| 608509 |
Alopecia Universalis Congenita, XY Gonadal Dysgenesis, and Laryngomalacia |
| 613490 |
Alpha-1-Antitrypsin Deficiency |
| 104250 |
Alpha-2c-Adrenergic Receptor; ADRA2C |
| 203760 |
Alpha-2-Deficient Collagen Disease |
| 614036 |
Alpha-2-Macroglobulin Deficiency; A2MD |
| 262850 |
Alpha-2-Plasmin Inhibitor Deficiency (1 mouse model) |
| 609889 |
Alpha/Beta T-Cell Lymphopenia with Gamma/Delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity |
| 104150 |
Alpha-Fetoprotein; AFP |
| 203740 |
Alpha-Ketoglutarate Dehydrogenase Deficiency |
| 203750 |
Alpha-Methylacetoacetic Aciduria |
| 614307 |
Alpha-Methylacyl-Coa Racemase Deficiency; AMACRD (1 mouse model) |
| 604131 |
Alpha-Thalassemia (7 mouse models) |
| 141750 |
Alpha-Thalassemia/Mental Retardation Syndrome, Chromosome 16-Related |
| 301040 |
Alpha-Thalassemia/Mental Retardation Syndrome, X-Linked; ATRX (3 mouse models) |
| 300448 |
Alpha-Thalassemia Myelodysplasia Syndrome; ATMDS |
| 104200 |
Alport Syndrome, Autosomal Dominant |
| 203780 |
Alport Syndrome, Autosomal Recessive (7 mouse models) |
| 301050 |
Alport Syndrome, X-Linked; ATS (2 mouse models) |
| 203800 |
Alstrom Syndrome; ALMS (3 mouse models) |
| 104290 |
Alternating Hemiplegia of Childhood 1; AHC1 |
| 614820 |
Alternating Hemiplegia of Childhood 2; AHC2 |
| 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 |
| 615080 |
Alzheimer Disease 17; AD17 |
| 104310 |
Alzheimer Disease 2 |
| 607822 |
Alzheimer Disease 3 (14 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 |
| 104300 |
Alzheimer Disease; AD (122 mouse models) |
| 605055 |
Alzheimer Disease, Familial Early-Onset, with Coexisting Amyloid and Prion Pathology |
| 607413 |
Alzheimer Disease Neuronal Thread Protein |
| 502500 |
Alzheimer Disease, Susceptibility to, Mitochondrial |
| 604154 |
Alzheimer Disease without Neurofibrillary Tangles |
| 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 |
| 614253 |
Amelogenesis Imperfecta and Gingival Fibromatosis Syndrome; AIGFS |
| 204700 |
Amelogenesis Imperfecta, Hypomaturation Type, Iia1; AI2A1 |
| 612529 |
Amelogenesis Imperfecta, Hypomaturation Type, Iia2; AI2A2 (1 mouse model) |
| 613211 |
Amelogenesis Imperfecta, Hypomaturation Type, Iia3; AI2A3 |
| 614832 |
Amelogenesis Imperfecta, Hypomaturation Type, Iia4; AI2A4 |
| 301201 |
Amelogenesis Imperfecta, Hypoplastic/Hypomaturation, X-Linked 2 |
| 104530 |
Amelogenesis Imperfecta, Hypoplastic Type (1 mouse model) |
| 104500 |
Amelogenesis Imperfecta, Type IB; AI1B (4 mouse models) |
| 204650 |
Amelogenesis Imperfecta, Type Ic; AI1C |
| 301200 |
Amelogenesis Imperfecta, Type IE; AI1E (6 mouse models) |
| 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 |
| 600325 |
Aminopterin Syndrome Sine Aminopterin; ASSA |
| 609056 |
Amish Infantile Epilepsy Syndrome |
| 300194 |
AMME Complex |
| 204800 |
Amobarbital, Deficient N-Hydroxylation of |
| 204900 |
Amyloidosis, Cutaneous Bullous |
| 105200 |
Amyloidosis, Familial Visceral |
| 105120 |
Amyloidosis, Finnish Type (2 mouse models) |
| 105210 |
Amyloidosis, Hereditary, Transthyretin-Related (2 mouse models) |
| 204850 |
Amyloidosis of Gingiva and Conjunctiva, with Mental Retardation |
| 105250 |
Amyloidosis, Primary Localized Cutaneous, 1; PLCA1 |
| 613955 |
Amyloidosis, Primary Localized Cutaneous, 2; PLCA2 |
| 205000 |
Amyotonia Congenita |
| 105300 |
Amyotrophic Dystonic Paraplegia |
| 612069 |
Amyotrophic Lateral Sclerosis 10, with or without Frontotemporal Dementia; (6 mouse models) |
| 612577 |
Amyotrophic Lateral Sclerosis 11; ALS11 |
| 613435 |
Amyotrophic Lateral Sclerosis 12; ALS12 |
| 613954 |
Amyotrophic Lateral Sclerosis 14, with or without Frontotemporal Dementia; |
| 300857 |
Amyotrophic Lateral Sclerosis 15, with or without Frontotemporal Dementia; |
| 614373 |
Amyotrophic Lateral Sclerosis 16, Juvenile; ALS16 |
| 614696 |
Amyotrophic Lateral Sclerosis 17; ALS17 |
| 614808 |
Amyotrophic Lateral Sclerosis 18; ALS18 |
| 105400 |
Amyotrophic Lateral Sclerosis 1; ALS1 (42 mouse models) |
| 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, with or without Frontotemporal Dementia; (1 mouse model) |
| 608031 |
Amyotrophic Lateral Sclerosis 7; ALS7 |
| 608627 |
Amyotrophic Lateral Sclerosis 8; ALS8 |
| 611895 |
Amyotrophic Lateral Sclerosis 9; ALS9 |
| 205200 |
Amyotrophic Lateral Sclerosis, Juvenile, with Dementia |
| 105500 |
Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1 |
| 205250 |
Amyotrophic Lateral Sclerosis with Polyglucosan Bodies |
| 162100 |
Amyotrophy, Hereditary Neuralgic; HNA |
| 602440 |
Amyotrophy, Monomelic |
| 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 |
| 312300 |
Androgen Insensitivity, Partial; PAIS |
| 300068 |
Androgen Insensitivity Syndrome; AIS (10 mouse models) |
| 300274 |
Androgen Insensitivity Syndrome Due to Coactivator Deficiency |
| 105570 |
Androstenone, Ability to Smell |
| 205700 |
Anemia, Autoimmune Hemolytic (2 mouse models) |
| 604315 |
Anemia, Congenital Hypoplastic, with Multiple Congenital Anomalies/Mental Retardation Syndrome |
| 224120 |
Anemia, Dyserythropoietic Congenital, Type I; CDAN1 |
| 224100 |
Anemia, Dyserythropoietic Congenital, Type II; CDAN2 (1 mouse model) |
| 105600 |
Anemia, Dyserythropoietic Congenital, Type III; CDAN3 |
| 613673 |
Anemia, Dyserythropoietic Congenital, Type IV; CDAN4 |
| 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 |
| 300835 |
Anemia, X-Linked, with or without Neutropenia and/or Platelet Abnormalities; |
| 206500 |
Anencephaly (5 mouse models) |
| 606179 |
Aneurysmal Bone Cysts |
| 612587 |
Aneurysm, Intracranial Berry, 10; ANIB10 |
| 614252 |
Aneurysm, Intracranial Berry, 11; ANIB11 |
| 105800 |
Aneurysm, Intracranial Berry, 1; ANIB1 |
| 608542 |
Aneurysm, Intracranial Berry, 2; ANIB2 |
| 609122 |
Aneurysm, Intracranial Berry, 3; ANIB3 |
| 610213 |
Aneurysm, Intracranial Berry, 4; ANIB4 |
| 300870 |
Aneurysm, Intracranial Berry, 5; ANIB5 |
| 611892 |
Aneurysm, Intracranial Berry, 6; ANIB6 |
| 612161 |
Aneurysm, Intracranial Berry, 7; ANIB7 |
| 612162 |
Aneurysm, Intracranial Berry, 8; ANIB8 |
| 612586 |
Aneurysm, Intracranial Berry, 9; ANIB9 |
| 105805 |
Aneurysm of Interventricular Septum |
| 105830 |
Angelman Syndrome; AS (4 mouse models) |
| 105835 |
Angel-Shaped Phalangoepiphyseal Dysplasia; ASPED |
| 106100 |
Angioedema, Hereditary, Type I; HAE1 |
| 610618 |
Angioedema, Hereditary, Type III; HAE3 |
| 607140 |
Angioid Streaks |
| 600419 |
Angiokeratoma Corporis Diffusum with Arteriovenous Fistulas |
| 206550 |
Angiolipomatosis, Familial |
| 106070 |
Angioma, Hereditary Neurocutaneous |
| 106050 |
Angioma Serpiginosum, Autosomal Dominant |
| 300652 |
Angioma Serpiginosum, X-Linked |
| 206570 |
Angiomatosis, Diffuse Corticomeningeal, of Divry and Van Bogaert |
| 607859 |
Angioma, Tufted |
| 611773 |
Angiopathy, Hereditary, with Nephropathy, Aneurysms, and Muscle Cramps; |
| 605910 |
Angiopoietin-Like 4; ANGPTL4 |
| 106180 |
Angiotensin I-Converting Enzyme; ACE |
| 106150 |
Angiotensinogen; AGT |
| 614081 |
Anhaptoglobinemia; AHP |
| 206600 |
Anhidrosis |
| 106190 |
Anhidrosis, Familial Generalized, with Normal Sweat Glands |
| 106210 |
Aniridia; AN (6 mouse models) |
| 106220 |
Aniridia and Absent Patella |
| 206700 |
Aniridia, Cerebellar Ataxia, and Mental Retardation |
| 106230 |
Aniridia, Microcornea, and Spontaneously Reabsorbed Cataract |
| 206750 |
Aniridia, Partial, with Unilateral Renal Agenesis and Psychomotor Retardation |
| 106240 |
Anisocoria |
| 605746 |
Anisomastia |
| 106260 |
Ankyloblepharon-Ectodermal Defects-Cleft Lip/Palate (1 mouse model) |
| 106250 |
Ankyloblepharon Filiforme Adnatum and Cleft Palate; AFA |
| 106280 |
Ankyloglossia (1 mouse model) |
| 106400 |
Ankylosing Vertebral Hyperostosis with Tylosis |
| 106500 |
Annular Erythema |
| 206780 |
Anodontia of Permanent Dentition |
| 106900 |
Anonychia-Ectrodactyly |
| 106990 |
Anonychia-Onychodystrophy with Brachydactyly Type B and Ectrodactyly |
| 106995 |
Anonychia-Onychodystrophy with Hypoplasia or Absence of Distal Phalanges |
| 607214 |
Anonychia, Total, with Microcephaly |
| 106750 |
Anonychia with Flexural Pigmentation |
| 107100 |
Anorectal Anomalies (1 mouse model) |
| 606788 |
Anorexia Nervosa, Susceptibility to, 1; ANON1 |
| 301700 |
Anosmia |
| 207000 |
Anosmia for Isobutyric Acid |
| 107200 |
Anosmia, Isolated Congenital; ANIC |
| 601427 |
Anterior Chamber Cleavage Disorder, Cerebellar Hypoplasia, Hypothyroidism, and Tracheal Stenosis |
| 107250 |
Anterior Segment Mesenchymal Dysgenesis; ASMD (7 mouse models) |
| 158030 |
Antigen Defined By Monoclonal Antibody Aj9 |
| 158040 |
Antigen Defined By Monoclonal Antibody T87 |
| 107320 |
Antiphospholipid Syndrome, Familial |
| 107290 |
Antipyrine Metabolism |
| 207300 |
Antithrombin, Familial Hemorrhagic Diathesis Due to |
| 613118 |
Antithrombin III Deficiency; AT3D (1 mouse model) |
| 107440 |
Antiviral State Repressor, Regulator Of; AVRR |
| 201750 |
Antley-Bixler Syndrome with Genital Anomalies and Disordered Steroidogenesis; |
| 207410 |
Antley-Bixler Syndrome without Genital Anomalies or Disordered Steroidogenesis; |
| 207500 |
Anus, Imperforate |
| 301800 |
Anus, Imperforate |
| 607834 |
Anxiety (2 mouse models) |
| 100070 |
Aortic Aneurysm, Familial Abdominal, 1; AAA1 |
| 609782 |
Aortic Aneurysm, Familial Abdominal, 2; AAA2 |
| 611891 |
Aortic Aneurysm, Familial Abdominal, 3; AAA3 |
| 614375 |
Aortic Aneurysm, Familial Abdominal, 4; AAA4 |
| 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 |
| 613780 |
Aortic Aneurysm, Familial Thoracic 7; AAT7 |
| 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; AOVD1 |
| 614823 |
Aortic Valve Disease 2; AOVD2 |
| 101200 |
Apert Syndrome (6 mouse models) |
| 610256 |
Aphakia, Congenital Primary |
| 600384 |
Aphalangia, Partial, with Syndactyly and Duplication of Metatarsal IV |
| 207620 |
Aphalangy with Hemivertebrae |
| 601075 |
Aplasia Cutis Congenita, High Myopia, and Cone-Rod Dysfunction |
| 107600 |
Aplasia Cutis Congenita, Nonsyndromic; ACC |
| 600360 |
Aplasia Cutis Congenita of Limbs, Autosomal Recessive |
| 300887 |
Aplasia Cutis Congenita, Reticulolinear, with Microcephaly, Facial Dysmorphism, and Other Congenital Anomalies; APLCC |
| 600268 |
Aplasia Cutis Congenita with Epibulbar Dermoids |
| 207731 |
Aplasia Cutis Congenita with Intestinal Lymphangiectasia |
| 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 |
| 107680 |
Apolipoprotein A-I; APOA1 |
| 107670 |
Apolipoprotein A-Ii; APOA2 |
| 152200 |
Apolipoprotein(a); LPA |
| 107730 |
Apolipoprotein B; APOB (8 mouse models) |
| 207750 |
Apolipoprotein C-II Deficiency |
| 107741 |
Apolipoprotein E; APOE (7 mouse models) |
| 218030 |
Apparent Mineralocorticoid Excess; AME (1 mouse model) |
| 107700 |
Appendicitis, Proneness to |
| 603119 |
Apraxia of Eyelid Opening |
| 601374 |
Aprosencephaly and Cerebellar Dysgenesis |
| 207770 |
Aprosencephaly Syndrome |
| 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 |
| 300261 |
Armfield X-Linked Mental Retardation Syndrome; MRXSA |
| 107850 |
Arm Folding Preference |
| 107900 |
Arms, Malformation of |
| 613546 |
Aromatase Deficiency |
| 139300 |
Aromatase Excess Syndrome; AEXS (1 mouse model) |
| 608643 |
Aromatic L-Amino Acid Decarboxylase Deficiency |
| 610193 |
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10; ARVD10 |
| 610476 |
Arrhythmogenic Right Ventricular Dysplasia, Familial, 11; ARVD11 |
| 611528 |
Arrhythmogenic Right Ventricular Dysplasia, Familial, 12; ARVD12 (2 mouse models) |
| 107970 |
Arrhythmogenic Right Ventricular Dysplasia, Familial, 1; ARVD1 |
| 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 (1 mouse model) |
| 604401 |
Arrhythmogenic Right Ventricular Dysplasia, Familial, 6; ARVD6 |
| 607450 |
Arrhythmogenic Right Ventricular Dysplasia, Familial, 8; ARVD8 |
| 609040 |
Arrhythmogenic Right Ventricular Dysplasia, Familial, 9; ARVD9 |
| 208000 |
Arterial Calcification, Generalized, of Infancy, 1; GACI1 |
| 614473 |
Arterial Calcification, Generalized, of Infancy, 2; GACI2 |
| 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 |
| 300158 |
Arthrogryposis, Congenital, Lower Limb, X-Linked; ACLLX |
| 187370 |
Arthrogryposis, Distal, Type 10; DA10 |
| 108120 |
Arthrogryposis, Distal, Type 1A; DA1A |
| 614335 |
Arthrogryposis, Distal, Type 1B; DA1B |
| 193700 |
Arthrogryposis, Distal, Type 2A; DA2A |
| 601680 |
Arthrogryposis, Distal, Type 2B; DA2B |
| 121070 |
Arthrogryposis, Distal, Type 2E |
| 114300 |
Arthrogryposis, Distal, Type 3; DA3 |
| 609128 |
Arthrogryposis, Distal, Type 4; DA4 |
| 108145 |
Arthrogryposis, Distal, Type 5; DA5 |
| 615065 |
Arthrogryposis, Distal, Type 5d; DA5D |
| 108200 |
Arthrogryposis, Distal, Type 6; DA6 |
| 158300 |
Arthrogryposis, Distal, Type 7; DA7 |
| 178110 |
Arthrogryposis, Distal, Type 8; DA8 |
| 121050 |
Arthrogryposis, Distal, Type 9; DA9 (3 mouse models) |
| 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 |
| 208200 |
Arthrogryposis-Like Disorder |
| 108110 |
Arthrogryposis Multiplex Congenita; AMC |
| 208100 |
Arthrogryposis Multiplex Congenita, Neurogenic Type; AMCN (1 mouse model) |
| 610001 |
Arthrogryposis Multiplex with Deafness, Inguinal Hernias, and Early Death |
| 614262 |
Arthrogryposis, Perthes Disease, and Upward Gaze Palsy; APUG |
| 208085 |
Arthrogryposis, Renal Dysfunction, and Cholestasis 1; ARCS1 |
| 613404 |
Arthrogryposis, Renal Dysfunction, and Cholestasis 2; ARCS2 |
| 208158 |
Arthrogryposis with Hyperkeratosis |
| 605935 |
Arthropathy, Erosive |
| 208230 |
Arthropathy, Progressive Pseudorheumatoid, of Childhood; PPAC |
| 108320 |
Artichoke, Modification of Taste By |
| 301835 |
Arts Syndrome; ARTS |
| 108340 |
Aryl Hydrocarbon Hydroxylase Inducibility |
| 604291 |
Ascaris Lumbricoides Infection, Susceptibility to |
| 208300 |
Ascites, Chylous |
| 108390 |
Asparagus, Specific Smell Hypersensitivity |
| 208400 |
Aspartylglucosaminuria; AGU (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; ASPGX1 |
| 300497 |
Asperger Syndrome, X-Linked, Susceptibility to, 2; ASPGX2 |
| 614079 |
Aspergillosis, Susceptibility to |
| 208500 |
Asphyxiating Thoracic Dystrophy 1; ATD1 (2 mouse models) |
| 611263 |
Asphyxiating Thoracic Dystrophy 2; ATD2 (1 mouse model) |
| 613091 |
Asphyxiating Thoracic Dystrophy 3; ATD3 (1 mouse model) |
| 613819 |
Asphyxiating Thoracic Dystrophy 4; ATD4 |
| 614376 |
Asphyxiating Thoracic Dystrophy 5; ATD5 |
| 608223 |
Aspirin Resistance |
| 271400 |
Asplenia, Isolated Congenital; ICAS |
| 208530 |
Asplenia with Cardiovascular Anomalies (3 mouse models) |
| 208550 |
Asthma, Nasal Polyps, and Aspirin Intolerance |
| 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 |
| 613207 |
Asthma-Related Traits, Susceptibility to, 8; ASRT8 |
| 208600 |
Asthma, Short Stature, and Elevated Iga |
| 600807 |
Asthma, Susceptibility to (7 mouse models) |
| 603047 |
Astigmatism |
| 108450 |
Asymmetric Short Stature Syndrome |
| 208750 |
Ataxia, Deafness, and Cardiomyopathy |
| 208850 |
Ataxia-Deafness-Retardation Syndrome |
| 208920 |
Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia; |
| 208870 |
Ataxia-Microcephaly-Cataract Syndrome |
| 608984 |
Ataxia, Sensory, 1, Autosomal Dominant; SNAX1 |
| 270500 |
Ataxia, Spastic, Childhood-Onset, Autosomal Recessive, with Optic Atrophy and Mental Retardation |
| 208900 |
Ataxia-Telangiectasia; AT (6 mouse models) |
| 604391 |
Ataxia-Telangiectasia-Like Disorder; ATLD |
| 208910 |
Ataxia-Telangiectasia with Generalized Skin Pigmentation and Early Death |
| 108700 |
Ataxia with Fasciculations |
| 208700 |
Ataxia with Myoclonic Epilepsy and Presenile Dementia |
| 108720 |
Atelosteogenesis, Type I; AOI |
| 256050 |
Atelosteogenesis, Type II; AOII |
| 108721 |
Atelosteogenesis, Type III; AOIII |
| 601536 |
Athabaskan Brainstem Dysgenesis Syndrome; ABDS (1 mouse model) |
| 209010 |
Atherosclerosis, Premature, with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease |
| 108725 |
Atherosclerosis Susceptibility; ATHS |
| 209050 |
Athrombia, Essential |
| 300431 |
Atkin-Flaitz Syndrome |
| 209100 |
Atonic-Astatic Syndrome of Foerster |
| 600046 |
ATP-Binding Cassette, Subfamily A, Member 1; ABCA1 |
| 516060 |
Atp Synthase 6; MTATP6 |
| 516070 |
Atp Synthase 8; MTATP8 |
| 209300 |
Atransferrinemia (2 mouse models) |
| 108760 |
Atresia of External Auditory Canal and Conductive Deafness |
| 614022 |
Atrial Fibrillation, Familial, 10; ATFB10 |
| 614049 |
Atrial Fibrillation, Familial, 11; ATFB11 |
| 614050 |
Atrial Fibrillation, Familial, 12; ATFB12 |
| 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 |
| 613980 |
Atrial Fibrillation, Familial, 9; ATFB9 |
| 108800 |
Atrial Septal Defect 1; ASD1 (5 mouse models) |
| 607941 |
Atrial Septal Defect 2; ASD2 (1 mouse model) |
| 614089 |
Atrial Septal Defect 3; ASD3 |
| 611363 |
Atrial Septal Defect 4; ASD4 |
| 612794 |
Atrial Septal Defect 5; ASD5 |
| 613087 |
Atrial Septal Defect 6; ASD6 |
| 108900 |
Atrial Septal Defect 7 with or without Atrioventricular Conduction Defects; ASD7 |
| 614433 |
Atrial Septal Defect 8; ASD8 |
| 614475 |
Atrial Septal Defect 9; ASD9 |
| 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 (3 mouse models) |
| 209600 |
Atrioventricular Dissociation |
| 600309 |
Atrioventricular Septal Defect 3; AVSD3 |
| 614430 |
Atrioventricular Septal Defect 4; AVSD4 |
| 614474 |
Atrioventricular Septal Defect 5; AVSD5 |
| 606215 |
Atrioventricular Septal Defect; AVSD (9 mouse models) |
| 606217 |
Atrioventricular Septal Defect, Susceptibility to, 2; AVSD2 |
| 600123 |
Atrioventricular Septal Defect with Blepharophimosis and Anal and Radial Defects |
| 601341 |
Atrophia Maculosa Varioliformis Cutis, Familial; AMVC |
| 209700 |
Atrophodermia Vermiculata |
| 143465 |
Attention Deficit-Hyperactivity Disorder; ADHD (4 mouse models) |
| 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 |
| 209950 |
Atypical Mycobacteriosis, Familial |
| 300636 |
Atypical Mycobacteriosis, Familial, X-Linked 1; AMCBX1 |
| 300645 |
Atypical Mycobacteriosis, Familial, X-Linked 2; AMCBX2 |
| 609129 |
Auditory Neuropathy, Autosomal Dominant, 1; AUNA1 |
| 607842 |
Aural Atresia, Congenital; CAA |
| 209770 |
Aural Atresia, Multiple Congenital Anomalies, and Mental Retardation |
| 602483 |
Auriculocondylar Syndrome 1; ARCND1 |
| 614669 |
Auriculocondylar Syndrome 2; ARCND2 |
| 109000 |
Auriculoosteodysplasia |
| 109050 |
Aurocephalosyndactyly |
| 209800 |
Australia Antigen |
| 209850 |
Autism (23 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 |
| 612100 |
Autism, Susceptibility to, 15; AUTS15 |
| 613410 |
Autism, Susceptibility to, 16; AUTS16 |
| 613436 |
Autism, Susceptibility to, 17; AUTS17 (2 mouse models) |
| 615032 |
Autism, Susceptibility to, 18; AUTS18 |
| 615091 |
Autism, Susceptibility to, 19; AUTS19 |
| 608049 |
Autism, Susceptibility to, 3; AUTS3 |
| 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, Susceptibility to, X-Linked 1; AUTSX1 (3 mouse models) |
| 300495 |
Autism, Susceptibility to, X-Linked 2; AUTSX2 |
| 300496 |
Autism, Susceptibility to, X-Linked 3; AUTSX3 |
| 300847 |
Autism, Susceptibility to, X-Linked 5; AUTSX5 |
| 109100 |
Autoimmune Disease (3 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 |
| 613551 |
Autoimmune Disease, Susceptibility to, 6; AIS6 |
| 613385 |
Autoimmune Disease, Syndromic Multisystem |
| 601859 |
Autoimmune Lymphoproliferative Syndrome; ALPS (4 mouse models) |
| 603909 |
Autoimmune Lymphoproliferative Syndrome, Type IIA; ALPS2A |
| 614470 |
Autoimmune Lymphoproliferative Syndrome, Type IV; ALPS4 |
| 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 |
| 614878 |
Autoinflammation, Antibody Deficiency, and Immune Dysregulation, Plcg2-Associated; |
| 256040 |
Autoinflammation, Lipodystrophy, and Dermatosis Syndrome; ALDD |
| 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 |
| 109160 |
Azotemia, Familial |
Analysis Tools