All diseases

OMIM ID
116860
OMIM term:
CEREBRAL CAVERNOUS MALFORMATIONS; CCM
Alternative terms:
CAVERNOUS ANGIOMA, FAMILIAL
CAVERNOUS ANGIOMATOUS MALFORMATIONS; CAM
CEREBRAL CAPILLARY MALFORMATIONS CEREBRAL CAVERNOUS MALFORMATIONS 1, INCLUDED; CCM1, INCLUDED
CAVERNOUS MALFORMATIONS OF CNS AND RETINA, INCLUDED
HYPERKERATOTIC CUTANEOUS CAPILLARY-VENOUS MALFORMATIONS ASSOCIATED WITH CEREBRAL CAPILLARY MALFORMATIONS, INCLUDED
(∗) Location:
7q21.2  
(†) Associated OMIM genes:
KRIT1  
(‡) Associated MGI genes:
Ccm2   Krit1  

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