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Congenital reticular ichthyosiform erythroderma

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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

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

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

Guidelines
Emergency guidelines
Français (2018.pdf) - Orphanet Urgences
Clinical practice guidelines
Français (2021) - PNDS Logo FSMR
English (2018) - Br J Dermatol Logo ERN
English (2019) - Br J Dermatol Logo ERN
Disease review articles
Review article
English (2015) - Orphanet J Rare Dis
Clinical genetics review
English (2013.pdf) - Eur J Hum Genet
Logo PROQOLID
Patient-Centered Outcome Measures (PCOMs)
Access questionnaires assessing quality of life in this disease (English)
Additional information

Further information on this disease

Patient-centred resources for this disease

Research activities on this disease

Newborn screening

The documents contained in this website are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.