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Erythrokeratodermia variabilis

ORPHA:317

Classification level: Disorder
  • Synonym(s):
    • EKV
    • Erythrokeratodermia variabilis, Mendes da Costa type
  • Prevalence: Unknown
  • Inheritance: Autosomal dominant or Autosomal recessive 
  • Age of onset: Infancy, Neonatal
  • ICD-10: Q82.8
  • ICD-11: EC20.0Y
  • OMIM: 133200  617524  617525  617526
  • UMLS: C0265961
  • MeSH: D056266
  • GARD: -
  • MedDRA: 10049048

Summary

This disease is described under Erythrokeratoderma variabilis progressiva

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

The documents contained in this web site 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.