Orphanet: MAGEL2 related Prader Willi like syndrome
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MAGEL2-related Prader-Willi-like syndrome

ORPHA:398069

Classification level: Disorder
  • Synonym(s):
    • MAGEL2-related PWLS
    • Schaaf-Yang syndrome
  • Prevalence: <1 / 1 000 000
  • Inheritance: Not applicable 
  • Age of onset: Neonatal
  • ICD-10: Q87.1
  • OMIM: 615547
  • UMLS: -
  • MeSH: -
  • GARD: -
  • MedDRA: -

Summary

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