All diseases

OMIM ID
163000
OMIM term:
CAPILLARY MALFORMATIONS, CONGENITAL, 1
Alternative terms:
CMC1
NEVI FLAMMEI, FAMILIAL MULTIPLE
PORT-WINE STAIN
CAPILLARY MALFORMATIONS; CMAL
(∗) Location:
5q13-q22  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/64s42orc