All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00998 - Miller-Dieker lissencephaly syndrome - - 0 0 PAFAH1B1 - -
02112 - Tyrosinemia type I 276700 - 1 1 FAH - -
00139 ID intellectual disability (ID) - - 1500 1237 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 528 more - -
02654 LIS-1 lissencephaly, type 1 (LIS-1) 607432 - 0 0 PAFAH1B1 - -
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