All diseases

OMIM ID
117650
OMIM term:
CEREBROCOSTOMANDIBULAR SYNDROME
Alternative terms:
CCM SYNDROME; CCMS
RIB GAP DEFECTS WITH MICROGNATHIA
(∗) Location:
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/4p50aa9y