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
00164 CFC1 CARDIOFACIOCUTANEOUS SYNDROME 1 115150 AD - - BRAF - -
00165 LPRD3 LEOPARD SYNDROME 3 613707 - - - BRAF - -
00166 NS7 NOONAN SYNDROME 7 613706 AD - - BRAF - -
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