Orphanet: KID syndrome

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KID syndrome

Disease definition

A rare congenital ectodermal disorder characterized by vascularizing keratitis, hyperkeratotic skin lesions and hearing loss.


Classification level: Disorder
  • Synonym(s):
    • Ichthyosis hystrix Rheydt type
    • KID/HID syndrome
    • Keratitis-ichthyosis-deafness/Hystrix-like ichthyosis-deafness syndrome
    • Senter syndrome
  • Prevalence: <1 / 1 000 000
  • Inheritance: Autosomal dominant or Not applicable or Autosomal recessive 
  • Age of onset: Neonatal
  • ICD-10: Q80.8
  • OMIM: 148210  242150  602540
  • UMLS: C0265336  C3665333
  • MeSH: -
  • GARD: 3113
  • MedDRA: 10048786

Detailed information


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