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
00787 - encephalopathy, neonatal, severe 300673 - - - MECP2 - -
00230 AS Angelman syndrome (AS) 105830 - - - CDKL5, MECP2, UBE3A - -
02161 AUTSX-3 autism, susceptibility to, X-linked, type 3 (AUTSX-3) 300496 - - - MECP2 - -
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 - -
04572 MRX-13 mental retardation, X-linked, syndromic, type 13 (MRX-13) 300055 - - - MECP2 - -
00788 MRXSL mental retardation, X-linked syndromic, Lubs type (MRXSL) 300260 - - - MECP2 - -
00066 RTT Rett syndrome (RTT) 312750 - - - MECP2 - -
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