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

Browse vocabulary terms by beginning character
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 0-9

Human Diseases/Syndromes Beginning with "A"

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

OMIM IDHuman Disease
OMIM:305400 Aarskog-Scott Syndrome; AAS
OMIM:100050 Aarskog Syndrome, Autosomal Dominant
OMIM:147800 Aase-Smith Syndrome I
OMIM:600501 Abcd Syndrome; ABCDS
OMIM:605552 Abdominal Obesity-Metabolic Syndrome 1; AOMS1
OMIM:615812 Abdominal Obesity-Metabolic Syndrome 3; AOMS3
OMIM:618620 Abdominal Obesity-Metabolic Syndrome 4; AOMS4
OMIM:605572 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2
OMIM:100200 Abducens Palsy
OMIM:200100 Abetalipoproteinemia; ABL
OMIM:300262 Abidi X-Linked Mental Retardation Syndrome; MRXSAB
OMIM:200110 Ablepharon-Macrostomia Syndrome; AMS
OMIM:261990 Abnormal Hair, Joint Laxity, and Developmental Delay; HJDD
OMIM:302905 Abruzzo-Erickson Syndrome; ABERS
OMIM:200130 Absent Eyebrows and Eyelashes with Mental Retardation
OMIM:100600 Acanthosis Nigricans
OMIM:200170 Acanthosis Nigricans with Muscle Cramps and Acral Enlargement
OMIM:614097 Acatalasemia
OMIM:614401 Accelerated Tumor Formation, Susceptibility To; ACTFS
OMIM:604290 Aceruloplasminemia
OMIM:200300 Acetophenetidin Sensitivity
OMIM:243400 Acetylation, Slow
OMIM:614055 Acetyl-Coa Acetyltransferase-2 Deficiency; ACAT2D
OMIM:613933 Acetyl-Coa Carboxylase Deficiency; ACACAD
OMIM:231550 Achalasia-Addisonianism-Alacrima Syndrome; AAAS
OMIM:200400 Achalasia, Familial Esophageal
OMIM:200450 Achalasia-Microcephaly Syndrome
OMIM:100700 Achard Syndrome
OMIM:200500 Acheiropody; ACHP
OMIM:200600 Achondrogenesis, Type IA; ACG1A
OMIM:600972 Achondrogenesis, Type IB; ACG1B
OMIM:200610 Achondrogenesis, Type II; ACG2
OMIM:100800 Achondroplasia; ACH
OMIM:616482 Achondroplasia, Severe, with Developmental Delay and Acanthosis Nigricans;
OMIM:100820 ACHOO Syndrome
OMIM:216900 Achromatopsia 2; ACHM2
OMIM:262300 Achromatopsia 3; ACHM3
OMIM:613856 Achromatopsia 4; ACHM4
OMIM:616517 Achromatopsia 7; ACHM7
OMIM:615961 Acid-Labile Subunit Deficiency; ACLSD
OMIM:200950 Acid Phosphatase Deficiency
OMIM:200970 Ackerman Syndrome
OMIM:604324 Acne, Adult
OMIM:142690 Acne Inversa, Familial, 1; ACNINV1
OMIM:613736 Acne Inversa, Familial, 2, with or without Dowling-Degos Disease;
OMIM:613737 Acne Inversa, Familial, 3; ACNINV3
OMIM:200990 Acrocallosal Syndrome; ACLS
OMIM:607778 Acrocapitofemoral Dysplasia; ACFD
OMIM:200995 Acrocephalopolydactylous Dysplasia
OMIM:101120 Acrocephalopolysyndactyly Type III
OMIM:201020 Acrocephalopolysyndactyly Type IV
OMIM:201050 Acrocraniofacial Dysostosis
OMIM:201100 Acrodermatitis Enteropathica, Zinc-Deficiency Type; AEZ
OMIM:101800 Acrodysostosis 1 with or without Hormone Resistance; ACRDYS1
OMIM:614613 Acrodysostosis 2 with or without Hormone Resistance; ACRDYS2
OMIM:603740 Acrodysplasia with Ossification Abnormalities, Short Stature, and Fibular Hypoplasia
OMIM:154400 Acrofacial Dysostosis 1, Nager Type; AFD1
OMIM:101805 Acrofacial Dysostosis, Catania Type
OMIM:616462 Acrofacial Dysostosis, Cincinnati Type; AFDCIN
OMIM:601829 Acrofacial Dysostosis, Palagonia Type
OMIM:201170 Acrofacial Dysostosis Syndrome of Rodriguez
OMIM:201180 Acrofrontofacionasal Dysostosis 1
OMIM:239710 Acrofrontofacionasal Dysostosis 2
OMIM:201200 Acrogeria, Gottron Type
OMIM:101840 Acrokeratoderma, Hereditary Papulotranslucent
OMIM:101900 Acrokeratosis Verruciformis; AKV
OMIM:102000 Acroleukopathy, Symmetric
OMIM:102100 Acromegaloid Changes, Cutis Verticis Gyrata, and Corneal Leukoma
OMIM:102150 Acromegaloid Facial Appearance Syndrome
OMIM:606049 Acromegaloid Features, Overgrowth, Cleft Palate, and Hernia
OMIM:603671 Acromelic Frontonasal Dysostosis; AFND
OMIM:609441 Acromesomelic Dysplasia, Demirhan Type; AMDD
OMIM:201250 Acromesomelic Dysplasia, Hunter-Thompson Type; AMDH
OMIM:602875 Acromesomelic Dysplasia, Maroteaux Type; AMDM
OMIM:102350 Acromial Dimples
OMIM:102370 Acromicric Dysplasia; ACMICD
OMIM:102400 Acroosteolysis
OMIM:605967 Acropectoral Syndrome; ACRPS
OMIM:102510 Acropectorovertebral Dysplasia; ACRPV
OMIM:200980 Acrorenal-Mandibular Syndrome
OMIM:102520 Acrorenal Syndrome
OMIM:201310 Acrorenal Syndrome, Autosomal Recessive
OMIM:201400 Acth Deficiency, Isolated; IAD
OMIM:615954 Acth-Independent Macronodular Adrenal Hyperplasia 2; AIMAH2
OMIM:219080 Acth-Independent Macronodular Adrenal Hyperplasia; AIMAH1
OMIM:174770 Actinic Prurigo
OMIM:617749 Actn3 Deficiency
OMIM:606752 Acute Hemorrhagic Leukoencephalitis
OMIM:601676 Acute Insulin Response
OMIM:612376 Acute Promyelocytic Leukemia; APL
OMIM:201450 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency Of; ACADMD
OMIM:201470 Acyl-Coa Dehydrogenase, Short-Chain, Deficiency Of; ACADSD
OMIM:201475 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency Of; ACADVLD
OMIM:102650 Adactylia, Unilateral
OMIM:102660 Adamantinoma of Long Bones
OMIM:100300 Adams-Oliver Syndrome 1; AOS1
OMIM:614219 Adams-Oliver Syndrome 2; AOS2
OMIM:614814 Adams-Oliver Syndrome 3; AOS3
OMIM:615297 Adams-Oliver Syndrome 4; AOS4
OMIM:616028 Adams-Oliver Syndrome 5; AOS5
OMIM:616589 Adams-Oliver Syndrome 6; AOS6
OMIM:201550 Adducted Thumbs Syndrome
OMIM:614723 Adenine Phosphoribosyltransferase Deficiency; APRTD
OMIM:600458 Adenomyosis
OMIM:102730 Adenosine Deaminase, Elevated, Hemolytic Anemia Due to
OMIM:102800 Adenosine Triphosphatase Deficiency, Anemia Due to
OMIM:102900 Adenosine Triphosphate, Elevated, of Erythrocytes
OMIM:612631 Adenylate Kinase Deficiency, Hemolytic Anemia Due to
OMIM:103050 Adenylosuccinase Deficiency; ADSLD
OMIM:136000 Adermatoglyphia; ADERM
OMIM:103100 Adie Pupil
OMIM:103200 Adiposis Dolorosa
OMIM:202110 Adrenal Hyperplasia, Congenital, Due to 17-Alpha-Hydroxylase Deficiency
OMIM:201910 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency
OMIM:201810 Adrenal Hyperplasia, Congenital, Due to 3-Beta-Hydroxysteroid Dehydrogenase 2 Deficiency
OMIM:202010 Adrenal Hyperplasia, Congenital, Due to Steroid 11-Beta-Hydroxylase Deficiency
OMIM:300200 Adrenal Hypoplasia, Congenital; AHC
OMIM:202150 Adrenal Hypoplasia, Congenital, with Absent Pituitary Luteinizing Hormone
OMIM:202155 Adrenal Hypoplasia, Cytomegalic Type
OMIM:613743 Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete
OMIM:202300 Adrenocortical Carcinoma, Hereditary; ADCC
OMIM:103230 Adrenocortical Hypofunction, Chronic Primary Congenital
OMIM:202355 Adrenocortical Unresponsiveness to ACTH with Postreceptor Defect
OMIM:300100 Adrenoleukodystrophy; ALD
OMIM:300270 Adrenomyodystrophy
OMIM:103285 ADULT Syndrome
OMIM:604348 Advanced Sleep Phase Syndrome, Familial, 1; FASPS1
OMIM:615224 Advanced Sleep Phase Syndrome, Familial, 2; FASPS2
OMIM:616882 Advanced Sleep Phase Syndrome, Familial, 3; FASPS3
OMIM:202400 Afibrinogenemia, Congenital
OMIM:601495 Agammaglobulinemia 1, Autosomal Recessive; AGM1
OMIM:613500 Agammaglobulinemia 2, Autosomal Recessive; AGM2
OMIM:613501 Agammaglobulinemia 3, Autosomal Recessive; AGM3
OMIM:613502 Agammaglobulinemia 4, Autosomal Recessive; AGM4
OMIM:613506 Agammaglobulinemia 5, Autosomal Dominant; AGM5
OMIM:612692 Agammaglobulinemia 6, Autosomal Recessive; AGM6
OMIM:615214 Agammaglobulinemia 7, Autosomal Recessive; AGM7
OMIM:616941 Agammaglobulinemia 8, Autosomal Dominant; AGM8
OMIM:610483 Agammaglobulinemia, Microcephaly, and Severe Dermatitis
OMIM:300755 Agammaglobulinemia, X-Linked; XLA
OMIM:202550 Aganglionosis, Total Intestinal
OMIM:202600 Agenesis of Cerebral White Matter
OMIM:618929 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome;
OMIM:613623 Agenesis of the Corpus Callosum and Congenital Lymphedema
OMIM:218000 Agenesis of the Corpus Callosum with Peripheral Neuropathy; ACCPN
OMIM:612448 Age-Related Hearing Impairment 1; ARHI1
OMIM:612976 Age-Related Hearing Impairment 2; ARHI2
OMIM:202650 Agnathia-Otocephaly Complex; AGOTC
OMIM:225750 Aicardi-Goutieres Syndrome 1; AGS1
OMIM:610181 Aicardi-Goutieres Syndrome 2; AGS2
OMIM:610329 Aicardi-Goutieres Syndrome 3; AGS3
OMIM:610333 Aicardi-Goutieres Syndrome 4; AGS4
OMIM:612952 Aicardi-Goutieres Syndrome 5; AGS5
OMIM:615010 Aicardi-Goutieres Syndrome 6; AGS6
OMIM:615846 Aicardi-Goutieres Syndrome 7; AGS7
OMIM:304050 Aicardi Syndrome; AIC
OMIM:608688 AICA-Ribosuria Due to ATIC Deficiency
OMIM:103400 Ainhum
OMIM:615510 Alacrima, Achalasia, and Mental Retardation Syndrome; AAMR
OMIM:103420 Alacrima, Congenital, Autosomal Dominant
OMIM:601549 Alacrima, Congenital, Autosomal Recessive
OMIM:118450 Alagille Syndrome 1; ALGS1
OMIM:610205 Alagille Syndrome 2; ALGS2
OMIM:300600 Aland Island Eye Disease; AIED
OMIM:202900 Alaninuria with Microcephaly, Dwarfism, Enamel Hypoplasia, and Diabetes Mellitus
OMIM:614687 Alar Cleft, Isolated
OMIM:615071 Alazami Syndrome; ALAZS
OMIM:617126 Alazami-Yuan Syndrome; ALYUS
OMIM:300700 Albinism-Deafness Syndrome; ADFN
OMIM:203340 Albinism-Microcephaly-Digital Anomalies Syndrome
OMIM:300500 Albinism, Ocular, Type I; OA1
OMIM:300650 Albinism, Ocular, with Late-Onset Sensorineural Deafness; OASD
OMIM:203100 Albinism, Oculocutaneous, Type IA; OCA1A
OMIM:606952 Albinism, Oculocutaneous, Type IB; OCA1B
OMIM:203290 Albinism, Oculocutaneous, Type III; OCA3
OMIM:203200 Albinism, Oculocutaneous, Type II; OCA2
OMIM:606574 Albinism, Oculocutaneous, Type IV; OCA4
OMIM:615179 Albinism, Oculocutaneous, Type VII; OCA7
OMIM:615312 Albinism, Oculocutaneous, Type V; OCA5
OMIM:103780 Alcohol Dependence
OMIM:610251 Alcohol Sensitivity, Acute
OMIM:100650 Aldehyde Dehydrogenase 2 Family; ALDH2
OMIM:203450 Alexander Disease; ALXDRD
OMIM:607131 Al-Gazali-Bakalinova Syndrome; AGBK
OMIM:609465 Al-Gazali Syndrome; ALGAZ
OMIM:617694 Al Kaissi Syndrome; ALKAS
OMIM:203500 Alkaptonuria; AKU
OMIM:617822 Alkuraya-Kucinskas Syndrome; ALKKUCS
OMIM:300523 Allan-Herndon-Dudley Syndrome; AHDS
OMIM:103920 Allergic Bronchopulmonary Aspergillosis, Familial
OMIM:607154 Allergic Rhinitis
OMIM:109200 Alopecia, Androgenetic, 1; AGA1
OMIM:300710 Alopecia, Androgenetic, 2; AGA2
OMIM:612421 Alopecia, Androgenetic, 3; AGA3
OMIM:104000 Alopecia Areata 1; AA1
OMIM:610753 Alopecia Areata 2; AA2
OMIM:300042 Alopecia, Congenital; ALPC
OMIM:203550 Alopecia-Contractures-Dwarfism Mental Retardation Syndrome
OMIM:203600 Alopecia-Epilepsy-Oligophrenia Syndrome of Moynahan
OMIM:104110 Alopecia, Familial Focal; ALPF
OMIM:203650 Alopecia-Mental Retardation Syndrome 1; APMR1
OMIM:610422 Alopecia-Mental Retardation Syndrome 2; APMR2
OMIM:613930 Alopecia-Mental Retardation Syndrome 3; APMR3
OMIM:618840 Alopecia-Mental Retardation Syndrome 4; APMR4
OMIM:601217 Alopecia-Mental Retardation Syndrome with Convulsions and Hypergonadotropic Hypogonadism
OMIM:612079 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome; ANES
OMIM:104130 Alopecia, Psychomotor Epilepsy, Pyorrhea, and Mental Subnormality
OMIM:203655 Alopecia Universalis Congenita; ALUNC
OMIM:608509 Alopecia Universalis Congenita, XY Gonadal Dysgenesis, and Laryngomalacia
OMIM:613490 Alpha-1-Antitrypsin Deficiency; A1ATD
OMIM:104250 Alpha-2c-Adrenergic Receptor; ADRA2C
OMIM:203760 Alpha-2-Deficient Collagen Disease
OMIM:614036 Alpha-2-Macroglobulin Deficiency; A2MD
OMIM:262850 Alpha-2-Plasmin Inhibitor Deficiency
OMIM:204750 Alpha-Aminoadipic and Alpha-Ketoadipic Aciduria; AAKAD
OMIM:609889 Alpha/Beta T-Cell Lymphopenia with Gamma/Delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity
OMIM:615969 Alpha-Fetoprotein Deficiency; AFPD
OMIM:615970 Alpha-Fetoprotein, Hereditary Persistence Of; HPAFP
OMIM:203740 Alpha-Ketoglutarate Dehydrogenase Deficiency
OMIM:203750 Alpha-Methylacetoacetic Aciduria
OMIM:614307 Alpha-Methylacyl-Coa Racemase Deficiency; AMACRD
OMIM:604131 Alpha-Thalassemia
OMIM:141750 Alpha-Thalassemia/Mental Retardation Syndrome, Chromosome 16-Related
OMIM:301040 Alpha-Thalassemia/Mental Retardation Syndrome, X-Linked; ATRX
OMIM:300448 Alpha-Thalassemia Myelodysplasia Syndrome; ATMDS
OMIM:301050 Alport Syndrome 1, X-Linked; ATS1
OMIM:203780 Alport Syndrome 2, Autosomal Recessive; ATS2
OMIM:104200 Alport Syndrome 3, Autosomal Dominant; ATS3
OMIM:616459 Al-Raqad Syndrome; ARS
OMIM:203800 Alstrom Syndrome; ALMS
OMIM:104290 Alternating Hemiplegia of Childhood 1; AHC1
OMIM:614820 Alternating Hemiplegia of Childhood 2; AHC2
OMIM:265380 Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins;
OMIM:606243 Alveolar Soft Part Sarcoma; ASPS
OMIM:619268 Alzahrani-Kuwahara Syndrome; ALKUS
OMIM:609636 Alzheimer Disease 10
OMIM:609790 Alzheimer Disease 11
OMIM:611073 Alzheimer Disease 12
OMIM:611152 Alzheimer Disease 13; AD13
OMIM:611154 Alzheimer Disease 14; AD14
OMIM:604154 Alzheimer Disease 15; AD15
OMIM:300756 Alzheimer Disease 16; AD16
OMIM:615080 Alzheimer Disease 17; AD17
OMIM:615590 Alzheimer Disease 18; AD18
OMIM:615711 Alzheimer Disease 19; AD19
OMIM:104310 Alzheimer Disease 2; AD2
OMIM:607822 Alzheimer Disease 3; AD
OMIM:606889 Alzheimer Disease 4
OMIM:602096 Alzheimer Disease 5
OMIM:605526 Alzheimer Disease 6
OMIM:606187 Alzheimer Disease 7
OMIM:607116 Alzheimer Disease 8
OMIM:608907 Alzheimer Disease 9, Susceptibility To; AD9
OMIM:104300 Alzheimer Disease; AD
OMIM:605055 Alzheimer Disease, Familial Early-Onset, with Coexisting Amyloid and Prion Pathology
OMIM:502500 Alzheimer Disease, Susceptibility to, Mitochondrial
OMIM:104350 Amastia, Bilateral, with Ureteral Triplication and Dysmorphism
OMIM:204110 Amaurosis Congenita, Cone-Rod Type, with Congenital Hypertrichosis
OMIM:619151 Amed Syndrome, Digenic; AMEDS
OMIM:604498 Amegakaryocytic Thrombocytopenia, Congenital; CAMT
OMIM:104400 Amelia and Terminal Transverse Hemimelia
OMIM:601360 Amelia, Posterior, with Pelvic and Pulmonary Hypoplasia Syndrome;
OMIM:204700 Amelogenesis Imperfecta, Hypomaturation Type, Iia1; AI2A1
OMIM:612529 Amelogenesis Imperfecta, Hypomaturation Type, Iia2; AI2A2
OMIM:613211 Amelogenesis Imperfecta, Hypomaturation Type, Iia3; AI2A3
OMIM:614832 Amelogenesis Imperfecta, Hypomaturation Type, Iia4; AI2A4
OMIM:615887 Amelogenesis Imperfecta, Hypomaturation Type, Iia5; AI2A5
OMIM:617217 Amelogenesis Imperfecta, Hypomaturation Type, Iia6; AI2A6
OMIM:301201 Amelogenesis Imperfecta, Hypoplastic/Hypomaturation, X-Linked 2
OMIM:104530 Amelogenesis Imperfecta, Type IA; AI1A
OMIM:104500 Amelogenesis Imperfecta, Type IB; AI1B
OMIM:204650 Amelogenesis Imperfecta, Type Ic; AI1C
OMIM:301200 Amelogenesis Imperfecta, Type IE; AI1E
OMIM:616270 Amelogenesis Imperfecta, Type IF; AI1F
OMIM:204690 Amelogenesis Imperfecta, Type IG; AI1G
OMIM:616221 Amelogenesis Imperfecta, Type IH; AI1H
OMIM:130900 Amelogenesis Imperfecta, Type IIIA; AI3A
OMIM:617607 Amelogenesis Imperfecta, Type IIIB; AI3B
OMIM:618386 Amelogenesis Imperfecta, Type Iiic; AI3C
OMIM:617297 Amelogenesis Imperfecta, Type IJ; AI1J
OMIM:104510 Amelogenesis Imperfecta, Type IV; AI4
OMIM:104570 Ameloonychohypohidrotic Syndrome
OMIM:104600 Amenorrhea-Galactorrhea Syndrome
OMIM:204730 Amino Aciduria with Mental Deficiency, Dwarfism, Muscular Dystrophy, Osteoporosis, and Acidosis
OMIM:609924 Aminoacylase 1 Deficiency; ACY1D
OMIM:600325 Aminopterin Syndrome Sine Aminopterin; ASSA
OMIM:300194 AMME Complex
OMIM:204800 Amobarbital, Deficient N-Hydroxylation of
OMIM:204900 Amyloidosis, Cutaneous Bullous
OMIM:105200 Amyloidosis, Familial Visceral
OMIM:105120 Amyloidosis, Finnish Type
OMIM:105210 Amyloidosis, Hereditary, Transthyretin-Related
OMIM:204850 Amyloidosis of Gingiva and Conjunctiva, with Mental Retardation
OMIM:105250 Amyloidosis, Primary Localized Cutaneous, 1; PLCA1
OMIM:613955 Amyloidosis, Primary Localized Cutaneous, 2; PLCA2
OMIM:617920 Amyloidosis, Primary Localized Cutaneous, 3; PLCA3
OMIM:205000 Amyotonia Congenita
OMIM:105300 Amyotrophic Dystonic Paraplegia
OMIM:612069 Amyotrophic Lateral Sclerosis 10 with or without Frontotemporal Dementia;
OMIM:612577 Amyotrophic Lateral Sclerosis 11; ALS11
OMIM:613435 Amyotrophic Lateral Sclerosis 12 with or without Frontotemporal Dementia; ALS12
OMIM:300857 Amyotrophic Lateral Sclerosis 15 with or without Frontotemporal Dementia; ALS15
OMIM:614373 Amyotrophic Lateral Sclerosis 16, Juvenile; ALS16
OMIM:614808 Amyotrophic Lateral Sclerosis 18; ALS18
OMIM:615515 Amyotrophic Lateral Sclerosis 19; ALS19
OMIM:105400 Amyotrophic Lateral Sclerosis 1; ALS1
OMIM:615426 Amyotrophic Lateral Sclerosis 20; ALS20
OMIM:606070 Amyotrophic Lateral Sclerosis 21; ALS21
OMIM:616208 Amyotrophic Lateral Sclerosis 22 with or without Frontotemporal Dementia;
OMIM:617839 Amyotrophic Lateral Sclerosis 23; ALS23
OMIM:619133 Amyotrophic Lateral Sclerosis 26 with or without Frontotemporal Dementia; ALS26
OMIM:205100 Amyotrophic Lateral Sclerosis 2, Juvenile; ALS2
OMIM:606640 Amyotrophic Lateral Sclerosis 3; ALS3
OMIM:602433 Amyotrophic Lateral Sclerosis 4, Juvenile; ALS4
OMIM:602099 Amyotrophic Lateral Sclerosis 5, Juvenile; ALS5
OMIM:608030 Amyotrophic Lateral Sclerosis 6 with or without Frontotemporal Dementia; ALS6
OMIM:608031 Amyotrophic Lateral Sclerosis 7; ALS7
OMIM:608627 Amyotrophic Lateral Sclerosis 8; ALS8
OMIM:611895 Amyotrophic Lateral Sclerosis 9; ALS9
OMIM:205200 Amyotrophic Lateral Sclerosis, Juvenile, with Dementia
OMIM:105500 Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1
OMIM:617892 Amyotrophic Lateral Sclerosis, Susceptibility to, 24; ALS24
OMIM:617921 Amyotrophic Lateral Sclerosis, Susceptibility to, 25; ALS25
OMIM:205250 Amyotrophic Lateral Sclerosis with Polyglucosan Bodies
OMIM:162100 Amyotrophy, Hereditary Neuralgic; HNA
OMIM:602440 Amyotrophy, Monomelic
OMIM:602553 Anal Atresia, Hypospadias, and Penoscrotal Inversion
OMIM:616000 Analbuminemia; ANALBA
OMIM:105580 Anal Canal Carcinoma
OMIM:105563 Anal Sphincter Dysplasia; ASDP
OMIM:105565 Anal Sphincter Myopathy, Internal
OMIM:607095 Anauxetic Dysplasia 1; ANXD1
OMIM:617396 Anauxetic Dysplasia 2; ANXD2
OMIM:618853 Anauxetic Dysplasia 3; ANXD3
OMIM:170390 Andersen Cardiodysrhythmic Periodic Paralysis
OMIM:312300 Androgen Insensitivity, Partial; PAIS
OMIM:300068 Androgen Insensitivity Syndrome; AIS
OMIM:205700 Anemia, Autoimmune Hemolytic
OMIM:224120 Anemia, Congenital Dyserythropoietic, Type IA; CDAN1A
OMIM:615631 Anemia, Congenital Dyserythropoietic, Type IB; CDAN1B
OMIM:224100 Anemia, Congenital Dyserythropoietic, Type II; CDAN2
OMIM:105600 Anemia, Congenital Dyserythropoietic, Type III; CDAN3
OMIM:613673 Anemia, Congenital Dyserythropoietic, Type IV; CDAN4
OMIM:604315 Anemia, Congenital Hypoplastic, with Multiple Congenital Anomalies/Mental Retardation Syndrome
OMIM:206100 Anemia, Hypochromic Microcytic, with Iron Overload 1; AHMIO1
OMIM:615234 Anemia, Hypochromic Microcytic, with Iron Overload 2; AHMIO2
OMIM:206300 Anemia, Nonspherocytic Hemolytic, Associated with Abnormality of Red Cell Membrane
OMIM:300908 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency
OMIM:206400 Anemia, Nonspherocytic Hemolytic, Possibly Due to Defect in Porphyrin Metabolism
OMIM:300751 Anemia, Sideroblastic, 1; SIDBA1
OMIM:205950 Anemia, Sideroblastic, 2, Pyridoxine-Refractory; SIDBA2
OMIM:616860 Anemia, Sideroblastic, 3, Pyridoxine-Refractory; SIDBA3
OMIM:182170 Anemia, Sideroblastic, 4; SIDBA4
OMIM:301310 Anemia, Sideroblastic, and Spinocerebellar Ataxia; ASAT
OMIM:206000 Anemia, Sideroblastic, Pyridoxine-Responsive, Autosomal Recessive
OMIM:300835 Anemia, X-Linked, with or without Neutropenia and/or Platelet Abnormalities; XLANP
OMIM:206500 Anencephaly; ANPH
OMIM:606179 Aneurysmal Bone Cysts
OMIM:612587 Aneurysm, Intracranial Berry, 10; ANIB10
OMIM:614252 Aneurysm, Intracranial Berry, 11; ANIB11
OMIM:618734 Aneurysm, Intracranial Berry, 12; ANIB12
OMIM:105800 Aneurysm, Intracranial Berry, 1; ANIB1
OMIM:608542 Aneurysm, Intracranial Berry, 2; ANIB2
OMIM:609122 Aneurysm, Intracranial Berry, 3; ANIB3
OMIM:610213 Aneurysm, Intracranial Berry, 4; ANIB4
OMIM:300870 Aneurysm, Intracranial Berry, 5; ANIB5
OMIM:611892 Aneurysm, Intracranial Berry, 6; ANIB6
OMIM:612161 Aneurysm, Intracranial Berry, 7; ANIB7
OMIM:612162 Aneurysm, Intracranial Berry, 8; ANIB8
OMIM:612586 Aneurysm, Intracranial Berry, 9; ANIB9
OMIM:105805 Aneurysm of Interventricular Septum
OMIM:105830 Angelman Syndrome; AS
OMIM:105835 Angel-Shaped Phalangoepiphyseal Dysplasia; ASPED
OMIM:106100 Angioedema, Hereditary, 1; HAE1
OMIM:610618 Angioedema, Hereditary, 3; HAE3
OMIM:619360 Angioedema, Hereditary, 4; HAE4
OMIM:619361 Angioedema, Hereditary, 5; HAE5
OMIM:619363 Angioedema, Hereditary, 6; HAE6
OMIM:619366 Angioedema, Hereditary, 7; HAE7
OMIM:619367 Angioedema, Hereditary, 8; HAE8
OMIM:300909 Angioedema Induced By Ace Inhibitors, Susceptibility To; AEACEI
OMIM:607140 Angioid Streaks
OMIM:600419 Angiokeratoma Corporis Diffusum with Arteriovenous Fistulas
OMIM:206550 Angiolipomatosis, Familial
OMIM:106070 Angioma, Hereditary Neurocutaneous
OMIM:106050 Angioma Serpiginosum, Autosomal Dominant
OMIM:300652 Angioma Serpiginosum, X-Linked
OMIM:206570 Angiomatosis, Diffuse Corticomeningeal, of Divry and Van Bogaert
OMIM:607859 Angioma, Tufted
OMIM:611773 Angiopathy, Hereditary, with Nephropathy, Aneurysms, and Muscle Cramps; HANAC
OMIM:106180 Angiotensin I-Converting Enzyme; ACE
OMIM:106150 Angiotensinogen; AGT
OMIM:614081 Anhaptoglobinemia; AHP
OMIM:206600 Anhidrosis, Familial Generalized, with Abnormal or Absent Sweat Glands
OMIM:106190 Anhidrosis, Isolated, with Normal Sweat Glands; ANHD
OMIM:106210 Aniridia 1; AN1
OMIM:617141 Aniridia 2; AN2
OMIM:617142 Aniridia 3; AN3
OMIM:106220 Aniridia and Absent Patella
OMIM:106230 Aniridia, Microcornea, and Spontaneously Reabsorbed Cataract
OMIM:206750 Aniridia, Partial, with Unilateral Renal Agenesis and Psychomotor Retardation
OMIM:106240 Anisocoria
OMIM:605746 Anisomastia
OMIM:106260 Ankyloblepharon-Ectodermal Defects-Cleft Lip/Palate; AEC
OMIM:106250 Ankyloblepharon Filiforme Adnatum and Cleft Palate; AFA
OMIM:106280 Ankyloglossia with or without Tooth Anomalies; ANKG
OMIM:106400 Ankylosing Vertebral Hyperostosis with Tylosis
OMIM:106500 Annular Erythema
OMIM:206780 Anodontia of Permanent Dentition
OMIM:106900 Anonychia-Ectrodactyly
OMIM:106990 Anonychia-Onychodystrophy with Brachydactyly Type B and Ectrodactyly
OMIM:106995 Anonychia-Onychodystrophy with Hypoplasia or Absence of Distal Phalanges
OMIM:607214 Anonychia, Total, with Microcephaly
OMIM:106750 Anonychia with Flexural Pigmentation
OMIM:107100 Anorectal Anomalies
OMIM:606788 Anorexia Nervosa, Susceptibility To; ANON
OMIM:270350 Anosmia for Butyl Mercaptan
OMIM:207000 Anosmia for Isobutyric Acid
OMIM:301700 Anosmia, Isolated Congenital
OMIM:107200 Anosmia, Isolated Congenital; ANIC
OMIM:601427 Anterior Chamber Cleavage Disorder, Cerebellar Hypoplasia, Hypothyroidism, and Tracheal Stenosis
OMIM:107250 Anterior Segment Dysgenesis 1; ASGD1
OMIM:610256 Anterior Segment Dysgenesis 2; ASGD2
OMIM:601631 Anterior Segment Dysgenesis 3; ASGD3
OMIM:137600 Anterior Segment Dysgenesis 4; ASGD4
OMIM:604229 Anterior Segment Dysgenesis 5; ASGD5
OMIM:617315 Anterior Segment Dysgenesis 6; ASGD6
OMIM:269400 Anterior Segment Dysgenesis 7; ASGD7
OMIM:617319 Anterior Segment Dysgenesis 8; ASGD8
OMIM:158030 Antigen Defined By Monoclonal Antibody Aj9
OMIM:158040 Antigen Defined By Monoclonal Antibody T87
OMIM:107254 Antigen Identified By Monoclonal Antibody 30.2a8; MIC12
OMIM:107260 Antigen Msk41 Identified By Monoclonal Antibody E3; MSK41
OMIM:107320 Antiphospholipid Syndrome, Familial
OMIM:107290 Antipyrine Metabolism
OMIM:207300 Antithrombin, Familial Hemorrhagic Diathesis Due to
OMIM:613118 Antithrombin III Deficiency; AT3D
OMIM:107440 Antiviral State Repressor, Regulator Of; AVRR
OMIM:201750 Antley-Bixler Syndrome with Genital Anomalies and Disordered Steroidogenesis; ABS1
OMIM:207410 Antley-Bixler Syndrome without Genital Anomalies or Disordered Steroidogenesis;
OMIM:207500 Anus, Imperforate
OMIM:301800 Anus, Imperforate
OMIM:607834 Anxiety
OMIM:100070 Aortic Aneurysm, Familial Abdominal, 1; AAA1
OMIM:609782 Aortic Aneurysm, Familial Abdominal, 2; AAA2
OMIM:611891 Aortic Aneurysm, Familial Abdominal, 3; AAA3
OMIM:614375 Aortic Aneurysm, Familial Abdominal, 4; AAA4
OMIM:617168 Aortic Aneurysm, Familial Thoracic 10; AAT10
OMIM:617349 Aortic Aneurysm, Familial Thoracic 11, Susceptibility To; AAT11
OMIM:607086 Aortic Aneurysm, Familial Thoracic 1; AAT1
OMIM:607087 Aortic Aneurysm, Familial Thoracic 2; AAT2
OMIM:132900 Aortic Aneurysm, Familial Thoracic 4; AAT4
OMIM:611788 Aortic Aneurysm, Familial Thoracic 6; AAT6
OMIM:613780 Aortic Aneurysm, Familial Thoracic 7; AAT7
OMIM:615436 Aortic Aneurysm, Familial Thoracic 8; AAT8
OMIM:616166 Aortic Aneurysm, Familial Thoracic 9; AAT9
OMIM:107500 Aortic Arch Anomaly with Peculiar Facies and Mental Retardation
OMIM:107550 Aortic Arch Interruption, Facial Palsy, and Retinal Coloboma
OMIM:109730 Aortic Valve Disease 1; AOVD1
OMIM:614823 Aortic Valve Disease 2; AOVD2
OMIM:618496 Aortic Valve Disease 3; AOVD3
OMIM:101200 Apert Syndrome
OMIM:600384 Aphalangia, Partial, with Syndactyly and Duplication of Metatarsal IV
OMIM:207620 Aphalangy with Hemivertebrae
OMIM:601075 Aplasia Cutis Congenita, High Myopia, and Cone-Rod Dysfunction
OMIM:107600 Aplasia Cutis Congenita, Nonsyndromic; ACC
OMIM:600360 Aplasia Cutis Congenita of Limbs, Autosomal Recessive
OMIM:207731 Aplasia Cutis Congenita with Intestinal Lymphangiectasia
OMIM:207740 Aplasia of Extensor Muscles of Fingers, Unilateral, with Generalized Polyneuropathy
OMIM:180920 Aplasia of Lacrimal and Salivary Glands; ALSG
OMIM:609135 Aplastic Anemia
OMIM:107640 Apnea, Central Sleep
OMIM:207720 Apnea, Central Sleep
OMIM:107650 Apnea, Obstructive Sleep
OMIM:107670 Apolipoprotein A-Ii; APOA2
OMIM:207750 Apolipoprotein C-II Deficiency
OMIM:614028 Apolipoprotein C-Iii Deficiency
OMIM:218030 Apparent Mineralocorticoid Excess; AME
OMIM:107700 Appendicitis, Proneness to
OMIM:603119 Apraxia of Eyelid Opening
OMIM:601374 Aprosencephaly and Cerebellar Dysgenesis
OMIM:207770 Aprosencephaly Syndrome
OMIM:207790 Arachnoid Cysts, Intracranial
OMIM:107750 Arbitrary Restriction Polymorphism 1
OMIM:616268 Arboleda-Tham Syndrome; ARTHS
OMIM:107800 Arcus Corneae
OMIM:207780 Aredyld
OMIM:207800 Argininemia
OMIM:207900 Argininosuccinic Aciduria
OMIM:243910 Arima Syndrome
OMIM:107900 Arms, Malformation of
OMIM:613546 Aromatase Deficiency
OMIM:139300 Aromatase Excess Syndrome; AEXS
OMIM:608643 Aromatic L-Amino Acid Decarboxylase Deficiency; AADCD
OMIM:610193 Arrhythmogenic Right Ventricular Dysplasia, Familial, 10; ARVD10
OMIM:610476 Arrhythmogenic Right Ventricular Dysplasia, Familial, 11; ARVD11
OMIM:611528 Arrhythmogenic Right Ventricular Dysplasia, Familial, 12; ARVD12
OMIM:615616 Arrhythmogenic Right Ventricular Dysplasia, Familial, 13; ARVD13
OMIM:618920 Arrhythmogenic Right Ventricular Dysplasia, Familial, 14; ARVD14
OMIM:107970 Arrhythmogenic Right Ventricular Dysplasia, Familial, 1; ARVD1
OMIM:600996 Arrhythmogenic Right Ventricular Dysplasia, Familial, 2; ARVD2
OMIM:602086 Arrhythmogenic Right Ventricular Dysplasia, Familial, 3; ARVD3
OMIM:602087 Arrhythmogenic Right Ventricular Dysplasia, Familial, 4; ARVD4
OMIM:604400 Arrhythmogenic Right Ventricular Dysplasia, Familial, 5; ARVD5
OMIM:604401 Arrhythmogenic Right Ventricular Dysplasia, Familial, 6; ARVD6
OMIM:607450 Arrhythmogenic Right Ventricular Dysplasia, Familial, 8; ARVD8
OMIM:609040 Arrhythmogenic Right Ventricular Dysplasia, Familial, 9; ARVD9
OMIM:208000 Arterial Calcification, Generalized, of Infancy, 1; GACI1
OMIM:614473 Arterial Calcification, Generalized, of Infancy, 2; GACI2
OMIM:600459 Arterial Dissection with Lentiginosis
OMIM:208050 Arterial Tortuosity Syndrome; ATORS
OMIM:108000 Arteries, Anomalies of
OMIM:208060 Arteriosclerosis, Severe Juvenile
OMIM:108010 Arteriovenous Malformations of the Brain
OMIM:108050 Arteritis, Familial Granulomatous, with Juvenile Polyarthritis
OMIM:108100 Arthritis, Sacroiliac
OMIM:601701 Arthrogryposis and Ectodermal Dysplasia
OMIM:618265 Arthrogryposis, Cleft Palate, Craniosynostosis, and Impaired Intellectual Development; ACCIID
OMIM:300158 Arthrogryposis, Congenital, Lower Limb, X-Linked; ACLLX
OMIM:187370 Arthrogryposis, Distal, Type 10; DA10
OMIM:108120 Arthrogryposis, Distal, Type 1A; DA1A
OMIM:614335 Arthrogryposis, Distal, Type 1B; DA1B
OMIM:619110 Arthrogryposis, Distal, Type 1C; DA1C
OMIM:193700 Arthrogryposis, Distal, Type 2A; DA2A
OMIM:601680 Arthrogryposis, Distal, Type 2B1; DA2B1
OMIM:618435 Arthrogryposis, Distal, Type 2B2; DA2B2
OMIM:618436 Arthrogryposis, Distal, Type 2b3; DA2B3
OMIM:121070 Arthrogryposis, Distal, Type 2E
OMIM:114300 Arthrogryposis, Distal, Type 3; DA3
OMIM:609128 Arthrogryposis, Distal, Type 4; DA4
OMIM:108145 Arthrogryposis, Distal, Type 5; DA5
OMIM:615065 Arthrogryposis, Distal, Type 5d; DA5D
OMIM:108200 Arthrogryposis, Distal, Type 6; DA6
OMIM:158300 Arthrogryposis, Distal, Type 7; DA7
OMIM:617146 Arthrogryposis, Distal, with Impaired Proprioception and Touch; DAIPT
OMIM:208081 Arthrogryposis, Distal, with Mental Retardation and Characteristic Facies
OMIM:301815 Arthrogryposis, Ectodermal Dysplasia, Cleft Lip/Palate, and Developmental Delay
OMIM:615553 Arthrogryposis, Mental Retardation, and Seizures; AMRS
OMIM:617468 Arthrogryposis Multiplex Congenita 1, Neurogenic, with Myelin Defect;
OMIM:208100 Arthrogryposis Multiplex Congenita 2, Neurogenic Type; AMC2
OMIM:618484 Arthrogryposis Multiplex Congenita 3, Myogenic Type; AMC3
OMIM:618766 Arthrogryposis Multiplex Congenita 4, Neurogenic, with Agenesis of the Corpus Callosum; AMC4
OMIM:618947 Arthrogryposis Multiplex Congenita 5; AMC5
OMIM:619334 Arthrogryposis Multiplex Congenita 6; AMC6
OMIM:610001 Arthrogryposis Multiplex with Deafness, Inguinal Hernias, and Early Death
OMIM:614262 Arthrogryposis, Perthes Disease, and Upward Gaze Palsy; APUG
OMIM:208085 Arthrogryposis, Renal Dysfunction, and Cholestasis 1; ARCS1
OMIM:613404 Arthrogryposis, Renal Dysfunction, and Cholestasis 2; ARCS2
OMIM:208158 Arthrogryposis with Hyperkeratosis
OMIM:605935 Arthropathy, Erosive
OMIM:301835 Arts Syndrome; ARTS
OMIM:604291 Ascaris Lumbricoides Infection, Susceptibility to
OMIM:208300 Ascites, Chylous
OMIM:615574 Asparagine Synthetase Deficiency; ASNSD
OMIM:208400 Aspartylglucosaminuria; AGU
OMIM:608638 Asperger Syndrome, Susceptibility to, 1; ASPG1
OMIM:608631 Asperger Syndrome, Susceptibility to, 2; ASPG2
OMIM:608781 Asperger Syndrome, Susceptibility to, 3; ASPG3
OMIM:609954 Asperger Syndrome, Susceptibility to, 4; ASPG4
OMIM:300494 Asperger Syndrome, X-Linked, Susceptibility to, 1; ASPGX1
OMIM:300497 Asperger Syndrome, X-Linked, Susceptibility to, 2; ASPGX2
OMIM:614079 Aspergillosis, Susceptibility to
OMIM:608223 Aspirin Resistance
OMIM:271400 Asplenia, Isolated Congenital; ICAS
OMIM:208550 Asthma, Nasal Polyps, and Aspirin Intolerance
OMIM:607277 Asthma-Related Traits, Susceptibility to, 1
OMIM:608584 Asthma-Related Traits, Susceptibility to, 2
OMIM:609958 Asthma-Related Traits, Susceptibility to, 3
OMIM:610906 Asthma-Related Traits, Susceptibility to, 4
OMIM:611064 Asthma-Related Traits, Susceptibility to, 5
OMIM:611403 Asthma-Related Traits, Susceptibility to, 6
OMIM:611960 Asthma-Related Traits, Susceptibility to, 7; ASRT7
OMIM:613207 Asthma-Related Traits, Susceptibility to, 8; ASRT8
OMIM:208600 Asthma, Short Stature, and Elevated Iga
OMIM:600807 Asthma, Susceptibility to
OMIM:603047 Astigmatism
OMIM:108450 Asymmetric Short Stature Syndrome
OMIM:500010 Ataxia and Polyneuropathy, Adult-Onset
OMIM:616192 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus; ACPHD
OMIM:208750 Ataxia, Deafness, and Cardiomyopathy
OMIM:208850 Ataxia-Deafness-Retardation Syndrome
OMIM:208920 Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia;
OMIM:619352 Ataxia, Intention Tremor, and Hypotonia Syndrome, Childhood-Onset;
OMIM:208870 Ataxia-Microcephaly-Cataract Syndrome
OMIM:615217 Ataxia-Oculomotor Apraxia 3; AOA3
OMIM:616267 Ataxia-Oculomotor Apraxia 4; AOA4
OMIM:159550 Ataxia-Pancytopenia Syndrome; ATXPC
OMIM:608984 Ataxia, Sensory, 1, Autosomal Dominant; SNAX1
OMIM:270500 Ataxia, Spastic, Childhood-Onset, Autosomal Recessive, with Optic Atrophy and Mental Retardation
OMIM:208900 Ataxia-Telangiectasia; AT
OMIM:604391 Ataxia-Telangiectasia-Like Disorder 1; ATLD1
OMIM:615919 Ataxia-Telangiectasia-Like Disorder 2; ATLD2
OMIM:208910 Ataxia-Telangiectasia with Generalized Skin Pigmentation and Early Death
OMIM:108700 Ataxia with Fasciculations
OMIM:208700 Ataxia with Myoclonic Epilepsy and Presenile Dementia
OMIM:277460 Ataxia with Vitamin 3 Deficiency; AVED
OMIM:108720 Atelosteogenesis, Type I; AO1
OMIM:256050 Atelosteogenesis, Type II; AO2
OMIM:108721 Atelosteogenesis, Type III; AO3
OMIM:601536 Athabaskan Brainstem Dysgenesis Syndrome; ABDS
OMIM:209010 Atherosclerosis, Premature, with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease
OMIM:108725 Atherosclerosis Susceptibility; ATHS
OMIM:209050 Athrombia, Essential
OMIM:300431 Atkin-Flaitz Syndrome
OMIM:209100 Atonic-Astatic Syndrome of Foerster
OMIM:209300 Atransferrinemia
OMIM:108760 Atresia of External Auditory Canal and Conductive Deafness
OMIM:614022 Atrial Fibrillation, Familial, 10; ATFB10
OMIM:614049 Atrial Fibrillation, Familial, 11; ATFB11
OMIM:614050 Atrial Fibrillation, Familial, 12; ATFB12
OMIM:615377 Atrial Fibrillation, Familial, 13; ATFB13
OMIM:615378 Atrial Fibrillation, Familial, 14; ATFB14
OMIM:615770 Atrial Fibrillation, Familial, 15; ATFB15
OMIM:617280 Atrial Fibrillation, Familial, 18; ATFB18
OMIM:608583 Atrial Fibrillation, Familial, 1; ATFB1
OMIM:608988 Atrial Fibrillation, Familial, 2; ATFB2
OMIM:607554 Atrial Fibrillation, Familial, 3; ATFB3
OMIM:611493 Atrial Fibrillation, Familial, 4; ATFB4
OMIM:611494 Atrial Fibrillation, Familial, 5; ATFB5
OMIM:612201 Atrial Fibrillation, Familial, 6; ATFB6
OMIM:612240 Atrial Fibrillation, Familial, 7; ATFB7
OMIM:613055 Atrial Fibrillation, Familial, 8; ATFB8
OMIM:613980 Atrial Fibrillation, Familial, 9; ATFB9
OMIM:108800 Atrial Septal Defect 1; ASD1
OMIM:607941 Atrial Septal Defect 2; ASD2
OMIM:614089 Atrial Septal Defect 3; ASD3
OMIM:611363 Atrial Septal Defect 4; ASD4
OMIM:612794 Atrial Septal Defect 5; ASD5
OMIM:613087 Atrial Septal Defect 6; ASD6
OMIM:108900 Atrial Septal Defect 7 with or without Atrioventricular Conduction Defects; ASD7
OMIM:614433 Atrial Septal Defect 8; ASD8
OMIM:614475 Atrial Septal Defect 9; ASD9
OMIM:603642 Atrial Septal Defect, Secundum, with Various Cardiac and Noncardiac Defects
OMIM:108770 Atrial Standstill 1; ATRST1
OMIM:615745 Atrial Standstill 2; ATRST2
OMIM:108950 Atrial Tachyarrhythmia with Short PR Interval
OMIM:209500 Atrichia with Papular Lesions; APL
OMIM:209600 Atrioventricular Dissociation
OMIM:600309 Atrioventricular Septal Defect 3; AVSD3
OMIM:614430 Atrioventricular Septal Defect 4; AVSD4
OMIM:614474 Atrioventricular Septal Defect 5; AVSD5
OMIM:606215 Atrioventricular Septal Defect; AVSD
OMIM:606217 Atrioventricular Septal Defect, Susceptibility to, 2; AVSD2
OMIM:600123 Atrioventricular Septal Defect with Blepharophimosis and Anal and Radial Defects
OMIM:601341 Atrophia Maculosa Varioliformis Cutis, Familial; AMVC
OMIM:209700 Atrophoderma Vermiculata; AVA
OMIM:108990 Attached Cell Antigen 28.3.7; MIC7
OMIM:143465 Attention Deficit-Hyperactivity Disorder; ADHD
OMIM:608903 Attention Deficit-Hyperactivity Disorder, Susceptibility to, 1
OMIM:608904 Attention Deficit-Hyperactivity Disorder, Susceptibility to, 2
OMIM:608905 Attention Deficit-Hyperactivity Disorder, Susceptibility to, 3
OMIM:608906 Attention Deficit-Hyperactivity Disorder, Susceptibility to, 4
OMIM:612311 Attention Deficit-Hyperactivity Disorder, Susceptibility to, 5
OMIM:612312 Attention Deficit-Hyperactivity Disorder, Susceptibility to, 6
OMIM:613003 Attention Deficit-Hyperactivity Disorder, Susceptibility to, 7
OMIM:617717 Auditory Neuropathy and Optic Atrophy; ANOA
OMIM:609129 Auditory Neuropathy, Autosomal Dominant, 1; AUNA1
OMIM:616580 Au-Kline Syndrome; AUKS
OMIM:607842 Aural Atresia, Congenital; CAA
OMIM:209770 Aural Atresia, Multiple Congenital Anomalies, and Mental Retardation
OMIM:602483 Auriculocondylar Syndrome 1; ARCND1
OMIM:614669 Auriculocondylar Syndrome 2; ARCND2
OMIM:615706 Auriculocondylar Syndrome 3; ARCND3
OMIM:109000 Auriculoosteodysplasia
OMIM:109050 Aurocephalosyndactyly
OMIM:209850 Autism
OMIM:611016 Autism, Susceptibility to, 10; AUTS10
OMIM:610836 Autism, Susceptibility to, 11; AUTS11
OMIM:610838 Autism, Susceptibility to, 12; AUTS12
OMIM:610908 Autism, Susceptibility to, 13; AUTS13
OMIM:612100 Autism, Susceptibility to, 15; AUTS15
OMIM:613410 Autism, Susceptibility to, 16; AUTS16
OMIM:613436 Autism, Susceptibility to, 17; AUTS17
OMIM:615032 Autism, Susceptibility to, 18; AUTS18
OMIM:615091 Autism, Susceptibility to, 19; AUTS19
OMIM:618830 Autism, Susceptibility to, 20; AUTS20
OMIM:608049 Autism, Susceptibility to, 3; AUTS3
OMIM:609378 Autism, Susceptibility to, 6; AUTS6
OMIM:610676 Autism, Susceptibility to, 7; AUTS7
OMIM:607373 Autism, Susceptibility to, 8; AUTS8
OMIM:611015 Autism, Susceptibility to, 9; AUTS9
OMIM:300425 Autism, Susceptibility to, X-Linked 1; AUTSX1
OMIM:300495 Autism, Susceptibility to, X-Linked 2; AUTSX2
OMIM:300496 Autism, Susceptibility to, X-Linked 3; AUTSX3
OMIM:300830 Autism, Susceptibility to, X-Linked 4; AUTSX4
OMIM:300847 Autism, Susceptibility to, X-Linked 5; AUTSX5
OMIM:300872 Autism, Susceptibility to, X-Linked 6; AUTSX6
OMIM:109100 Autoimmune Disease
OMIM:615952 Autoimmune Disease, Multisystem, Infantile-Onset, 1; ADMIO1
OMIM:617006 Autoimmune Disease, Multisystem, Infantile-Onset, 2; ADMIO2
OMIM:613385 Autoimmune Disease, Multisystem, with Facial Dysmorphism; ADMFD
OMIM:607836 Autoimmune Disease, Susceptibility to, 1; AIS1
OMIM:608391 Autoimmune Disease, Susceptibility to, 2; AIS2
OMIM:608392 Autoimmune Disease, Susceptibility to, 3; AIS3
OMIM:609400 Autoimmune Disease, Susceptibility to, 4; AIS4
OMIM:613551 Autoimmune Disease, Susceptibility to, 6; AIS6
OMIM:616414 Autoimmune Interstitial Lung, Joint, and Kidney Disease; AILJK
OMIM:601859 Autoimmune Lymphoproliferative Syndrome; ALPS
OMIM:603909 Autoimmune Lymphoproliferative Syndrome, Type IIA; ALPS2A
OMIM:615559 Autoimmune Lymphoproliferative Syndrome, Type III; ALPS3
OMIM:616100 Autoimmune Lymphoproliferative Syndrome, Type V; ALPS5
OMIM:269200 Autoimmune Polyendocrine Syndrome, Type II; APS2
OMIM:240300 Autoimmune Polyendocrine Syndrome, Type I, with or without Reversible Metaphyseal Dysplasia; APS1
OMIM:608173 Autoimmune Thyroid Disease, Susceptibility to, 1
OMIM:608174 Autoimmune Thyroid Disease, Susceptibility to, 2
OMIM:608175 Autoimmune Thyroid Disease, Susceptibility to, 3; AITD3
OMIM:608176 Autoimmune Thyroid Disease, Susceptibility to, 4
OMIM:614878 Autoinflammation, Antibody Deficiency, and Immune Dysregulation;
OMIM:618999 Autoinflammation, Immune Dysregulation, and Eosinophilia; AIIDE
OMIM:617099 Autoinflammation, Panniculitis, and Dermatosis Syndrome; AIPDS
OMIM:617388 Autoinflammation with Arthritis and Dyskeratosis; AIADK
OMIM:618852 Autoinflammation with Episodic Fever and Lymphadenopathy; AIEFL
OMIM:616050 Autoinflammation with Infantile Enterocolitis; AIFEC
OMIM:616744 Autoinflammatory Syndrome, Familial, Behcet-Like; AISBL
OMIM:619375 Autoinflammatory Syndrome, Familial, with or without Immunodeficiency; AISIMD
OMIM:109110 Autonomously Replicating Sequence 1
OMIM:608805 Avascular Necrosis of Femoral Head, Primary, 1; ANFH1
OMIM:617383 Avascular Necrosis of Femoral Head, Primary, 2; ANFH2
OMIM:109120 Axenfeld-Rieger Anomaly with Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, and Skeletal Abnormalities
OMIM:180500 Axenfeld-Rieger Syndrome, Type 1; RIEG1
OMIM:601499 Axenfeld-Rieger Syndrome, Type 2; RIEG2
OMIM:602482 Axenfeld-Rieger Syndrome, Type 3; RIEG3
OMIM:109130 Axial Osteomalacia
OMIM:601088 Ayme-Gripp Syndrome; AYGRP
OMIM:301060 Azoospermia, Obstructive, with Nephrolithiasis; OAZON
OMIM:109160 Azotemia, Familial

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.17
The Jackson Laboratory