- OMIM ID
-
182212
- OMIM term:
- SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME
- Alternative terms:
-
SGS
CRANIOSYNOSTOSIS WITH ARACHNODACTYLY AND ABDOMINAL HERNIAS
MARFANOID DISORDER WITH CRANIOSYNOSTOSIS, TYPE I
MARFANOID CRANIOSYNOSTOSIS SYNDROME
- (∗) Location:
- 15q21.1
- (†) Associated OMIM genes:
- FBN1
- (‡) Associated MGI genes:
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