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"

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OMIM ID	Human 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: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:619959	Acces Syndrome; ACCES
OMIM:604290	Aceruloplasminemia; ACEP
OMIM:200300	Acetophenetidin Sensitivity
OMIM:243400	Acetylation, Slow
OMIM:614055	Acetyl-Coa Acetyltransferase-2 Deficiency; ACAT2D
OMIM:613933	Acetyl-Coa Carboxylase-Alpha 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; SADDAN
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:602875	Acromesomelic Dysplasia 1; AMD1
OMIM:200700	Acromesomelic Dysplasia 2A; AMD2A
OMIM:228900	Acromesomelic Dysplasia 2B; AMD2B
OMIM:201250	Acromesomelic Dysplasia 2c; AMD2C
OMIM:609441	Acromesomelic Dysplasia 3; AMD3
OMIM:619636	Acromesomelic Dysplasia 4; AMD4
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:314100	Adducted Thumbs, Congenital
OMIM:201550	Adducted Thumbs Syndrome
OMIM:614723	Adenine Phosphoribosyltransferase Deficiency; APRTD
OMIM:600458	Adenomyosis
OMIM:301083	Adenosine Deaminase, Elevated, Hemolytic Anemia Due To; HAEADA
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:620015	Advance Sleep Phase Syndrome, Familial, 4; FASPS4
OMIM:202400	Afibrinogenemia, Congenital
OMIM:619707	Agammaglobulinemia 10, Autosomal Dominant; AGM10
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 8a, Autosomal Dominant; AGM8A
OMIM:619824	Agammaglobulinemia 8b, Autosomal Recessive; AGM8B
OMIM:619693	Agammaglobulinemia 9, Autosomal Recessive; AGM9
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:619486	Aicardi-Goutieres Syndrome 8; AGS8
OMIM:619487	Aicardi-Goutieres Syndrome 9; AGS9
OMIM:304050	Aicardi Syndrome; AIC
OMIM:608688	Aica-Ribosiduria Due to Atic Deficiency
OMIM:103400	Ainhum
OMIM:615510	Alacrima, Achalasia, and Impaired Intellectual Development Syndrome;
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:620655	Alfadhel Syndrome; AFDL
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-Intellectual Disability Syndrome 1; APMR1
OMIM:610422	Alopecia-Intellectual Disability Syndrome 2; APMR2
OMIM:613930	Alopecia-Intellectual Disability Syndrome 3; APMR3
OMIM:618840	Alopecia-Intellectual Disability 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:203750	Alpha-Methylacetoacetic Aciduria
OMIM:614307	Alpha-Methylacyl-Coa Racemase Deficiency; AMACRD
OMIM:604131	Alpha-Thalassemia
OMIM:141750	Alpha-Thalassemia/Impaired Intellectual Development Syndrome, Deletion Type
OMIM:301040	Alpha-Thalassemia/Impaired Intellectual Development 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 3a, Autosomal Dominant; ATS3A
OMIM:620536	Alport Syndrome 3b, Autosomal Recessive; ATS3B
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; AD3
OMIM:606889	Alzheimer Disease 4; AD4
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, Familial, 1; AD1
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, 1; CAMT1
OMIM:620481	Amegakaryocytic Thrombocytopenia, Congenital, 2; CAMT2
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:620104	Amelogenesis Imperfecta, Type IK; AI1K
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 Impaired Intellectual Development
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:620285	Amyotrophic Lateral Sclerosis 27, Juvenile; ALS27
OMIM:620452	Amyotrophic Lateral Sclerosis 28; ALS28
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 IIIA; CDAN3A
OMIM:619789	Anemia, Congenital Dyserythropoietic, Type Iiib, Autosomal Recessive;
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:619523	Anemia, Sideroblastic, 5; SIDBA5
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 1; ANPH1
OMIM:619452	Anencephaly 2; ANPH2
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:107200	Anosmia, Isolated Congenital; ANIC
OMIM:301700	Anosmia, Isolated Congenital, X-Linked
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:619825	Aortic Aneurysm, Familial Thoracic 12; AAT12
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:207720	Apnea, Central Sleep
OMIM:107640	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:620519	Arrhythmogenic Cardiomyopathy with Variable Ectodermal Abnormalities;
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: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:620019	Arthrogryposis, Distal, Type 11; DA11
OMIM:620545	Arthrogryposis, Distal, Type 12; DA12
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:208081	Arthrogryposis, Distal, with Impaired Intellectual Development and Characteristic Facies
OMIM:617146	Arthrogryposis, Distal, with Impaired Proprioception and Touch; DAIPT
OMIM:301815	Arthrogryposis, Ectodermal Dysplasia, Cleft Lip/Palate, and Developmental Delay
OMIM:615553	Arthrogryposis, Impaired Intellectual Development, 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: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 E Deficiency; AVED
OMIM:620184	Atelis Syndrome 1; ATELS1
OMIM:620185	Atelis Syndrome 2; ATELS2
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: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:619957	Attention Deficit-Hyperactivity Disorder 8; ADHD8
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; ADHD7
OMIM:617717	Auditory Neuropathy and Optic Atrophy; ANOA
OMIM:609129	Auditory Neuropathy, Autosomal Dominant 1; AUNA1
OMIM:620384	Auditory Neuropathy, Autosomal Dominant 2; AUNA2
OMIM:619832	Auditory Neuropathy, Autosomal Dominant 3; AUNA3
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 2A; ARCND2A
OMIM:620458	Auriculocondylar Syndrome 2B; ARCND2B
OMIM:615706	Auriculocondylar Syndrome 3; ARCND3
OMIM:620457	Auriculocondylar Syndrome 4; ARCND4
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: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:620430	Autoimmune Disease, Multisystem, Infantile-Onset, 3; ADMIO3
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: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:620296	Autoinflammation with Pulmonary and Cutaneous Vasculitis; AIPCV
OMIM:618287	Autoinflammatory Disease, Familial, Behcet-Like 3; AIFBL3
OMIM:301109	Autoinflammatory Disease, Multisystem, with Immune Dysregulation, X-Linked; ADMIDX
OMIM:620376	Autoinflammatory Disease, Systemic, with Vasculitis; SAIDV
OMIM:301081	Autoinflammatory Disease, Systemic, X-Linked; SAIDX
OMIM:619858	Autoinflammatory-Pancytopenia Syndrome; AIPCS
OMIM:616744	Autoinflammatory Syndrome, Familial, Behcet-Like 1; AIFBL1
OMIM:619375	Autoinflammatory Syndrome, Familial, with or without Immunodeficiency; AISIMD
OMIM:301074	Autoinflammatory Syndrome, Familial, X-Linked, Behcet-Like 2; AIFBL2
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

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