All diseases

OMIM ID
211750
OMIM term:
C SYNDROME
Alternative terms:
OPITZ TRIGONOCEPHALY SYNDROME
TRIGONOCEPHALY SYNDROME
(∗) Location:
3q13.1-q13.2  
(†) Associated OMIM genes:
CD96  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/xz1mzwre