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List of all diseases starting with A

• ABETALIPOPROTEINEMIA, BASSEN-KORNZWEIG-SYNDROME, ACANTHOCYTOSIS (ABL) MIM=200100
• ACATALASEMIA MIM=614097
• ACERULOPLASMINEMIA MIM=604290
• ACETYL-CoA ACETYLTRANSFERASE-2 DEFICIENCY; ACAT2D MIM=614055
• ACETYL-CoA CARBOXYLASE DEFICIENCY; ACACAD MIM=613933
• ACRODERMATITIS ENTEROHEPATHICA MIM=201100
• ACTH DEFICIENCY, ISOLATED MIM=201400
• ACUTE INTERMITTEND PORPHYRIA (AIP) MIM=176000
• ADENINE PHOSPHORIBOSYLTRANSFERASE DEFICIENCY (APRT) MIM=614723
• ADENOSINE DEAMINASE (ADA-SCID) MIM=102700
• ADENOSINE KINASE DEFICIENCY MIM=614300
• ADENYLATE KINASE DEFICIENCY, HEMOLYTIC ANEMIA DUE TO MIM=612631
• ADENYLOSUCCINASE DEFICIENCY (ADSL) MIM=103050
• ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 17-ALPHA-HYDROXYLASE DEFICIENCY MIM=202110
• ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY (CAH) MIM=201910
• ADRENAL HYPOPLASIA. ADDISON DISEASE, X-LINKED MIM=300200
• ADRENAL INSUFFICIENCY, CONGENITAL, WITH 46,XY SEX REVERSAL, PARTIAL OR COMPLETE MIM=613743
• ADRENOLEUKODYSTROPHY, X-LINKED MIM=300100
• AICAR TRANSFORMYLASE/IMP CYCLOHYDROLASE DEFICIENCY (ATIC) MIM=608688
• AICARDI-GOUTIERES SYNDROME 5; AGS5 MIM=612952
• ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME (CDG) MIM=615510
• ALEXANDER DISEASE MIM=203450
• ALKAPTONURIA (AKU) MIM=203500
• ALLAN-HERNDON-DUDLEY SYNDROME; AHDS MIM=300523
• ALPHA-1-ANTITRYPSIN DEFICIENCY (AATD) MIM=613490
• ALPHA-AMINO-ADIPIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY (AAASAD) MIM=266100
• ALPHA-MANNOSIDOSIS MIM=248500
• ALPHA-METHYLACYL-CoA RACEMASE DEFICIENCY (AMACRD) MIM=614307
• ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY TYPE II: , KANZAKI DISEASE MIM=609242
• ALPORT SYNDROME MIM=301050
• AMINOACYLASE I DEFICIENCY (ACY1D) MIM=609924
• AMISH LETHAL MICROCEPHALY; THIAMINE METABOLISM DYSFUNCTION SYNDROME 3 (MICROCEPHALY TYPE) MIM=607196
• ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE II; CDAN2 MIM=224100
• ANEMIA, SIDEROBLASTIC, 1; SIDBA1 MIM=300751
• ANEMIA, SIDEROBLASTIC, 2, PYRIDOXINE-REFRACTORY; SIDBA2 MIM=205950
• ANEMIA, SIDEROBLASTIC, AND SPINOCEREBELLAR ATAXIA (ASAT) MIM=301310
• ANTI-NMDA RECEPTOR ENCEPHALITIS [DD] MIM=---
• ANTICONVULSANT HYPERSENSITIVITY SYNDROME : CARBAMAZEPINE [EXTERNAL] MIM=---
• ANTICONVULSANT HYPERSENSITIVITY SYNDROME : VALPROATE ASSOCIATED HEPATOTOXICITY [DD] MIM=---
• ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS; ABS1 MIM=201750
• APOLIPOPROTEIN C-II DEFICIENCY MIM=207750
• APPARENT MINERALOCORTICOID EXCESS (AME) MIM=218030
• ARGININEMIA MIM=207800
• ARGININOSUCCINIC ACIDURIA (ASL) MIM=207900
• AROMATASE DEFICIENCY MIM=613546
• AROMATASE EXCESS SYNDROME (AEXS) MIM=139300
• AROMATIC L-AMINO ACID DECARBOXYLASE DEFICIENCY (AADC) MIM=608643
• ARTERIAL TORTUOSITY SYNDROME (ATS) MIM=208050
• ARTS SYNDROME; ARTS MIM=301835
• ASPARAGINE SYNTHETASE DEFICIENCY (ASNSD) MIM=615574
• ASPARTYLGLUCOSAMINURIA (AGU) MIM=208400
• ASPHYXIA [DD] MIM=---
• ATAXIA-OCULOMOTOR APRAXIA 3; AOA3 MIM=615217
• ATRANSFERRINEMIA MIM=209300
• AUTISM MIM=209850
• AUTISM SPECTRUM DISORDERS (ASD) [DD] MIM=---
• AUTISM, SUSCEPTIBILITY TO, X-LINKED 6 (AUTSX6) MIM=300872