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Congenital reticular ichthyosiform erythroderma

ORPHA:281190

Classification level: Disorder
  • Synonym(s):
    • CRIE
    • IWC
    • Ichthyosis variegata
    • Ichthyosis with confetti
  • Prevalence: <1 / 1 000 000
  • Inheritance: Autosomal dominant 
  • Age of onset: Neonatal
  • ICD-10: Q80.8
  • ICD-11: EC20.0Y
  • OMIM: 609165
  • UMLS: C3665704
  • MeSH: -
  • GARD: -
  • MedDRA: -

Summary

An Orphanet summary for this disease is currently under development. However, other data related to the disease are accessible from the Additional Information menu located at the bottom of this page.

Detailed information

Guidelines

Disease review articles

Clinical Outcome Assessment (COA)

  • Patient-Centered Outcome Measures (PCOMs)
  • English (2023) - PROQOLIDTM
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

Research activities on this disease

Specialised Social Services

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