Orphanet: Mowat Wilson syndrome due to monosomy 2q22
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Mowat-Wilson syndrome due to monosomy 2q22

ORPHA:261537

Classification level: Subtype of disorder
  • Synonym(s):
    • Hirschsprung disease and intellectual disability due to 2q22 microdeletion
    • Hirschsprung disease and intellectual disability due to del(2)(q22)
    • Hirschsprung disease and intellectual disability due to monosomy 2q22
    • Mowat-Wilson syndrome due to 2q22 microdeletion
    • Mowat-Wilson syndrome due to del(2)q(22)
  • Prevalence: -
  • Inheritance: -
  • Age of onset: -
  • ICD-10: Q43.1
  • OMIM: 235730
  • UMLS: -
  • MeSH: -
  • GARD: -
  • MedDRA: -

Summary

This disease is described under Mowat-Wilson syndrome

  A summary on this disease is available in

Detailed information

General public

Guidelines

ERN : produced/endorsed by ERN(s)
FSMR : produced/endorsed by FSMR(s)

Additional information

Further information on this disease

Patient-centred resources for this disease

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