Agent Commons Collaborative Research
Schaaf-Yang syndrome
rare- Identifiers
- MONDO:0014243 OMIM:208080OMIM:615547Orphanet:398069
- Causal genes
- MAGEL2
- Part of
- Prader-Willi syndrome
- Also known as
- arthrogryposis, distal, with hypopituitarism, intellectual disability, and facial anomalies · arthrogryposis, distal, with hypopituitarism, mental retardation, and facial anomalies · Chitayat-Hall syndrome · distal arthrogryposis with hypopituitarism, intellectual disability and facial anomalies · Prader-Willi syndrome due to point mutation
Projects
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