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Concept information

disease > immunopathology > inflammation > keratitis > KID syndrome
... > disease > eye disease > anterior segment disease > keratopathy > keratitis > KID syndrome
disease > complex syndrome > KID syndrome
... > disease > nervous system diseases > neurological disorder > auditory disorder > hearing loss > KID syndrome
disease > ENT disease > auditory disorder > hearing loss > KID syndrome
... > disease > skin appendages disease > skin disease > dyskeratosis > hyperkeratosis > ichthyosis > KID syndrome

Preferred term

KID syndrome  

Definition(s)

  • Keratitis–ichthyosis–deafness syndrome (also known as "Ichthyosiform erythroderma, corneal involvement, and deafness," and "KID syndrome,") presents at birth/infancy and is characterized by progressive corneal opacification, either mild generalized hyperkeratosis or discrete erythematous plaques, and neurosensory deafness.It is caused by a mutation in connexin 26. (Wikipedia)

Broader concept(s)

Synonym(s)

  • keratitis ichthyosis deafness syndrome

In other languages

URI

http://data.loterre.fr/ark:/67375/VH8-HMRW6MZQ-3

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