- OMIM ID
-
305450
- OMIM term:
- OPITZ-KAVEGGIA SYNDROME; OKS
- Alternative terms:
-
FG SYNDROME 1; FGS1
FG SYNDROME; FGS
MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA, AND PARTIAL AGENESIS OF CORPUS CALLOSUM
KELLER SYNDROME
- (∗) Location:
- Xq13.1
- (†) Associated OMIM genes:
- MED12
- (‡) Associated MGI genes:
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