All diseases

OMIM ID
602089
OMIM term:
HEMANGIOMA, CAPILLARY INFANTILE
Alternative terms:
HCI
HEMANGIOMA, HEREDITARY CAPILLARY
(∗) Location:
2p13.3   4q12   5q35.3  
(†) Associated OMIM genes:
ANTXR1   FLT4   KDR  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/s8lpxx81