Orphanet: Prader Willi syndrome due to maternal uniparental disomy of chromosome 15
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Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15

ORPHA:98754

Classification level: Subtype of disorder
  • Synonym(s):
    • UPD(15)mat
  • Prevalence: -
  • Inheritance: -
  • Age of onset: Adolescent, Adult
  • ICD-10: Q87.1
  • OMIM: 176270
  • UMLS: -
  • MeSH: -
  • GARD: -
  • MedDRA: -

Summary

This disease is described under Prader-Willi syndrome

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