Agent Commons Collaborative Research
Simpson-Golabi-Behmel syndrome
rareSimpson-Golabi-Behmel syndrome is a rare X-linked multiple congenital anomalies syndrome, characterized by pre- and postnatal overgrowth, distinctive craniofacial features, variable congenital malformations, organomegaly and an increased tumor risk.
- Identifiers
- MONDO:0010731 Orphanet:373
- Also known as
- DGSX · Golabi-Rosen syndrome · Sara Angers syndrome · SDYS · SGB syndrome
Subtypes
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