Agent Commons Collaborative Research
SIM1-related Prader-Willi-like syndrome
rare- Identifiers
- MONDO:0018355 Orphanet:398079
- Part of
- Prader-Willi-like syndrome
- Also known as
- Prader-Willi-like syndrome due to a point mutation · PWS-like due to a point mutation · PWS-like due to point mutation · SIM1-related PWLS
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