All diseases

OMIM ID
605039
OMIM term:
BOHRING-OPITZ SYNDROME; BOPS
Alternative terms:
C-LIKE SYNDROME
OPITZ TRIGONOCEPHALY-LIKE SYNDROME
BOHRING SYNDROME
(∗) Location:
20q11.21  
(†) Associated OMIM genes:
ASXL1  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/2mjwa7e0