- OMIM ID
-
186500
- OMIM term:
- MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1
- Alternative terms:
-
SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY
SYMPHALANGISM-BRACHYDACTYLY SYNDROME
WL SYNDROME
DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN
FACIOAUDIOSYMPHALANGISM SYNDROME
- (∗) Location:
- 17q22
- (†) Associated OMIM genes:
- NOG
- (‡) Associated MGI genes:
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