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
04638 CMD-1NN cardiomyopathy, dilated, type 1NN (CMD-1NN) 615916 - - - RAF1 - -
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 - -
00576 LPRD-2 LEOPARD syndrome, type 2 (LPRD-2) 611554 - - - RAF1 - -
00575 NS-5 Noonan syndrome, type 5 (NS-5) 611553 - - - RAF1 - -
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