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Cutis verticis gyrata-intellectual disability syndrome

ORPHA:1557

  • Synonym(s):
    • McDowall syndrome
  • Prevalence: -
  • Inheritance: -
  • Age of onset: -
  • ICD-10: -
  • OMIM: 219300
  • UMLS: -
  • MeSH: -
  • GARD: 3425
  • MedDRA: -

Summary

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Primary non-essential cutis verticis gyrata

Additional information

Further information on this disease

Patient-centred resources for this disease

Research activities on this disease

Specialised Social Services

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