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Human Disease Vocabulary Browser
The current vocabulary contains human disease, syndrome, and condition terms from Online Mendelian Inheritance in Man (OMIM database).

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Human Diseases/Syndromes Beginning with "A"

To see all annotations for a disease, click the disease name.

OMIM IDHuman 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 1; AOMS1
615812 Abdominal Obesity-Metabolic Syndrome 3; AOMS3
605572 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2
100200 Abducens Palsy
200100 Abetalipoproteinemia; ABL
300262 Abidi X-Linked Mental Retardation Syndrome; MRXSAB
200110 Ablepharon-Macrostomia Syndrome
302905 Abruzzo-Erickson Syndrome; ABERS
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)
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 models)
200600 Achondrogenesis, Type IA; ACG1A (1 mouse models)
600972 Achondrogenesis, Type IB; ACG1B
200610 Achondrogenesis, Type II; ACG2 (1 mouse models)
100800 Achondroplasia; ACH (13 mouse models)
100820 ACHOO Syndrome
216900 Achromatopsia 2; ACHM2 (1 mouse models)
262300 Achromatopsia 3; ACHM3
613856 Achromatopsia 4; ACHM4 (1 mouse models)
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 (1 mouse models)
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 models)
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 (1 mouse models)
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 models)
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
612376 Acute Promyelocytic Leukemia; APL (5 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 models)
201470 Acyl-Coa Dehydrogenase, Short-Chain, Deficiency Of; ACADSD (1 mouse models)
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
615297 Adams-Oliver Syndrome 4; AOS4
201550 Adducted Thumbs Syndrome
614723 Adenine Phosphoribosyltransferase Deficiency; APRTD (3 mouse models)
600458 Adenomyosis
102730 Adenosine Deaminase, Elevated, Hemolytic Anemia Due to
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 models)
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, 1; FASPS1 (1 mouse models)
615224 Advanced Sleep Phase Syndrome, Familial, 2; FASPS2 (2 mouse models)
202400 Afibrinogenemia, Congenital (1 mouse models)
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
615214 Agammaglobulinemia 7, Autosomal Recessive; AGM7
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 models)
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
615846 Aicardi-Goutieres Syndrome 7; AGS7
304050 Aicardi Syndrome; AIC
608688 Aicar Transformylase/Imp Cyclohydrolase Deficiency
103400 Ainhum
615510 Alacrima, Achalasia, and Mental Retardation Syndrome; AAMR
103420 Alacrima, Congenital
601549 Alacrima, Congenital, Autosomal Recessive
118450 Alagille Syndrome 1; ALGS1 (5 mouse models)
610205 Alagille Syndrome 2; ALGS2
300600 Aland Island Eye Disease; AIED
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 models)
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 models)
606952 Albinism, Oculocutaneous, Type IB; OCA1B (1 mouse models)
203290 Albinism, Oculocutaneous, Type III; OCA3
203200 Albinism, Oculocutaneous, Type II; OCA2
606574 Albinism, Oculocutaneous, Type IV; OCA4 (7 mouse models)
615179 Albinism, Oculocutaneous, Type VII; OCA7
615312 Albinism, Oculocutaneous, Type V; OCA5
103600 Albumin; ALB
103780 Alcohol Dependence (1 mouse models)
610251 Alcohol Sensitivity, Acute
100650 Aldehyde Dehydrogenase 2 Family; ALDH2
203450 Alexander Disease (7 mouse models)
609465 Al-Gazali Syndrome
203500 Alkaptonuria; AKU (1 mouse models)
300523 Allan-Herndon-Dudley Syndrome; AHDS (1 mouse models)
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 (1 mouse models)
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 models)
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 models)
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; (2 mouse models)
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
615590 Alzheimer Disease 18; AD18
615711 Alzheimer Disease 19; AD19
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 (135 mouse models)
605055 Alzheimer Disease, Familial Early-Onset, with Coexisting Amyloid and Prion Pathology
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 models)
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 models)
613211 Amelogenesis Imperfecta, Hypomaturation Type, Iia3; AI2A3
614832 Amelogenesis Imperfecta, Hypomaturation Type, Iia4; AI2A4
615887 Amelogenesis Imperfecta, Hypomaturation Type, Iia5; AI2A5
301201 Amelogenesis Imperfecta, Hypoplastic/Hypomaturation, X-Linked 2
104530 Amelogenesis Imperfecta, Hypoplastic Type (1 mouse models)
104500 Amelogenesis Imperfecta, Type IB; AI1B (4 mouse models)
204650 Amelogenesis Imperfecta, Type Ic; AI1C
301200 Amelogenesis Imperfecta, Type IE; AI1E (6 mouse models)
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
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; (7 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
615515 Amyotrophic Lateral Sclerosis 19; ALS19
105400 Amyotrophic Lateral Sclerosis 1; ALS1 (48 mouse models)
615426 Amyotrophic Lateral Sclerosis 20; ALS20
606070 Amyotrophic Lateral Sclerosis 21; ALS21
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; (2 mouse models)
608031 Amyotrophic Lateral Sclerosis 7; ALS7
608627 Amyotrophic Lateral Sclerosis 8; ALS8 (1 mouse models)
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 (1 mouse models)
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)
224120 Anemia, Congenital Dyserythropoietic, Type IA; CDAN1A
615631 Anemia, Congenital Dyserythropoietic, Type IB; CDAN1B
224100 Anemia, Congenital Dyserythropoietic, Type II; CDAN2 (1 mouse models)
105600 Anemia, Congenital Dyserythropoietic, Type III; CDAN3
613673 Anemia, Congenital Dyserythropoietic, Type IV; CDAN4
604315 Anemia, Congenital Hypoplastic, with Multiple Congenital Anomalies/Mental Retardation Syndrome
206100 Anemia, Hypochromic Microcytic, with Iron Overload 1; AHMIO1
615234 Anemia, Hypochromic Microcytic, with Iron Overload 2; AHMIO2
206300 Anemia, Nonspherocytic Hemolytic, Associated with Abnormality of Red Cell Membrane
300908 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency
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
300909 Angioedema Induced By Ace Inhibitors, Susceptibility To; AEACEI
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;
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 models)
106250 Ankyloblepharon Filiforme Adnatum and Cleft Palate; AFA
106280 Ankyloglossia (1 mouse models)
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 models)
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 models)
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
615436 Aortic Aneurysm, Familial Thoracic 8; AAT8
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
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
207720 Apnea, Central Sleep
107640 Apnea, Central Sleep
107650 Apnea, Obstructive Sleep
107680 Apolipoprotein A-I; APOA1
107670 Apolipoprotein A-Ii; APOA2
107730 Apolipoprotein B; APOB (8 mouse models)
207750 Apolipoprotein C-II Deficiency
107741 Apolipoprotein E; APOE (8 mouse models)
218030 Apparent Mineralocorticoid Excess; AME (1 mouse models)
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
207800 Argininemia (1 mouse models)
207900 Argininosuccinic Aciduria (2 mouse models)
603457 Arhinia, Choanal Atresia, and Microphthalmia
243910 Arima Syndrome
300261 Armfield X-Linked Mental Retardation Syndrome; MRXSA
107900 Arms, Malformation of
613546 Aromatase Deficiency
139300 Aromatase Excess Syndrome; AEXS (1 mouse models)
608643 Aromatic L-Amino Acid Decarboxylase Deficiency (1 mouse models)
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)
615616 Arrhythmogenic Right Ventricular Dysplasia, Familial, 13; ARVD13
107970 Arrhythmogenic Right Ventricular Dysplasia, Familial, 1; ARVD1
600996 Arrhythmogenic Right Ventricular Dysplasia, Familial, 2; ARVD2 (1 mouse models)
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 models)
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 (1 mouse models)
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 models)
108000 Arteries, Anomalies of
208060 Arteriosclerosis, Severe Juvenile
108010 Arteriovenous Malformations of the Brain (3 mouse models)
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
615553 Arthrogryposis, Mental Retardation, and Seizures; AMRS
108110 Arthrogryposis Multiplex Congenita; AMC
208100 Arthrogryposis Multiplex Congenita, Neurogenic Type; AMCN (1 mouse models)
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
604291 Ascaris Lumbricoides Infection, Susceptibility to
208300 Ascites, Chylous
615574 Asparagine Synthetase Deficiency; ASNSD
108390 Asparagus, Specific Smell Hypersensitivity
208400 Aspartylglucosaminuria; AGU (2 mouse models)
608638 Asperger Syndrome, Susceptibility to, 1; ASPG1
608631 Asperger Syndrome, Susceptibility to, 2; ASPG2
608781 Asperger Syndrome, Susceptibility to, 3; ASPG3
609954 Asperger Syndrome, Susceptibility to, 4; ASPG4
300494 Asperger Syndrome, X-Linked, Susceptibility to, 1; ASPGX1
300497 Asperger Syndrome, X-Linked, Susceptibility to, 2; ASPGX2
614079 Aspergillosis, Susceptibility to
608223 Aspirin Resistance
271400 Asplenia, Isolated Congenital; ICAS
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
615217 Ataxia-Oculomotor Apraxia 3; AOA3
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 1; ATLD1
615919 Ataxia-Telangiectasia-Like Disorder 2; ATLD2
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; AO1
256050 Atelosteogenesis, Type II; AO2
108721 Atelosteogenesis, Type III; AO3
601536 Athabaskan Brainstem Dysgenesis Syndrome; ABDS (1 mouse models)
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
615377 Atrial Fibrillation, Familial, 13; ATFB13
615378 Atrial Fibrillation, Familial, 14; ATFB14
615770 Atrial Fibrillation, Familial, 15; ATFB15
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 models)
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 1; ATRST1
615745 Atrial Standstill 2; ATRST2
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 Atrophoderma Vermiculata; AVA
143465 Attention Deficit-Hyperactivity Disorder; ADHD (10 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 (2 mouse models)
607842 Aural Atresia, Congenital; CAA
209770 Aural Atresia, Multiple Congenital Anomalies, and Mental Retardation
602483 Auriculocondylar Syndrome 1; ARCND1
614669 Auriculocondylar Syndrome 2; ARCND2
615706 Auriculocondylar Syndrome 3; ARCND3
109000 Auriculoosteodysplasia
109050 Aurocephalosyndactyly
209850 Autism (32 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 models)
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
269200 Autoimmune Polyendocrine Syndrome, Type II; APS2
240300 Autoimmune Polyendocrine Syndrome, Type I, with or without Reversible Metaphyseal Dysplasia; APS1 (9 mouse models)
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 (9 mouse models)
601499 Axenfeld-Rieger Syndrome, Type 2; RIEG2
602482 Axenfeld-Rieger Syndrome, Type 3; RIEG3 (1 mouse models)
109130 Axial Osteomalacia
109160 Azotemia, Familial

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last database update
08/19/2014
MGI 5.19
The Jackson Laboratory