All diseases

OMIM ID
233500
OMIM term:
GORLIN-CHAUDHRY-MOSS SYNDROME
Alternative terms:
GCM SYNDROME
CRANIOFACIAL DYSOSTOSIS, HYPERTRICHOSIS, HYPOPLASIA OF LABIA MAJORA,
DENTAL AND EYE ANOMALIES, PATENT DUCTUS ARTERIOSUS, AND NORMAL INTELLIGENCE
(∗) Location:
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/del1lgz4