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
00640 CFC1 cardiofaciocutaneous syndrome, type 1 (CFC-1) 115150 AD 3 3 BRAF, KRAS, MAP2K1, MAP2K2 - -
03882 CFC4 cardiofaciocutaneous syndrome, type 4 (CFC-4) 615280 AD - - MAP2K2 - -
00139 ID intellectual disability (ID) - - 2695 2377 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 553 more - -
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