All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01117 - mental retardation, X-linked syndromic, Fried type 300630 - 0 0 AP1S2 - -
02229 - Dandy-Walker malformation, mental retardation, basal ganglia disease, seizures (Pettigrew syndrome, MRXS-5) 304340 - 0 0 AP1S2 - -
00139 ID intellectual disability (ID) - - 1846 1579 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 536 more - -
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