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Hyperkeratosis lenticularis perstans

ORPHA:409

Classification level: Disorder
  • Synonym(s):
    • Flegel disease
  • Prevalence: Unknown
  • Inheritance: Autosomal dominant or Not applicable 
  • Age of onset: Adult
  • ICD-10: -
  • OMIM: 144150
  • UMLS: C0263420
  • MeSH: C538377
  • GARD: 2824
  • MedDRA: 10071311

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.

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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.