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
02551 BCC1 carcinoma, basal cell, susceptibility to, type 1 (BCC-1) 605462 - 10 10 PTCH1, PTCH2, RASA1, SMO - -
06904 CMAVM capillary malformation-arteriovenous malformation - - 1 1 EPHB4, RASA1 - -
02753 CMAVM1 capillary malformation-arteriovenous malformation, type 1 608354 AD 122 122 RASA1 - autosomal dominant
02754 PKWS Parkes Weber syndrome (PKWS) 608355 - - - RASA1 - -
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