All diseases

7 entries on 1 page. Showing entries 1 - 7.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01058 - Proud syndrome 300004 - - - ARX - -
00264 EIEE-1 encephalopathy, epileptic, early infantile, type 1 (EIEE-1) 308350 - - - ARX - -
00139 ID intellectual disability (ID) - - - - AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 515 more - -
00187 IDX (MRX) intellectual disability, X-linked (IDX, mental retardation (MRX)) - - - - ARX, IL1RAPL1 - -
00266 LISX-2;XLAG lissencephaly, X-linked, type 2 (LISX-2, with ambiguous genitalia (XLAG)) 300215 - - - ARX - -
01057 MRX-29 mental retardation, X-linked, type 29 and others (MRX-29) 300419 - - - ARX - -
00265 PRTS mental retardation, Partington syndrome (PRTS) 309510 - - - ARX - -
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