KID syndrome

MONDO:0018781

Keratitis (and hystrix-like) ichthyosis deafness (KID/HID) syndrome is a rare congenital ectodermal disorder characterized by vascularizing keratitis, hyperkeratotic skin lesions and hearing loss.

Also known as: KID/HID syndrome, Keratitis Ichthyosis Deafness Syndrome, Senter syndrome, ichthyosis hystrix Rheydt type, keratitis-ichthyosis-deafness/Hystrix-like ichthyosis-deafness syndrome, keratitis, ichthyosis, and deafness (KID) syndrome

0 clinical trials for this condition and its sub-types, 0 tagged with KID syndrome itself.

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Part of

↑ Ectodermal dysplasia syndrome (45) ↑ Diffuse palmoplantar keratoderma (12)

Sub-types of KID syndrome

Autosomal dominant keratitis-ichthyosis-hearing loss syndrome 0 trials
Ichthyosiform erythroderma, corneal involvement, and hearing loss 0 trials
Ichthyosis, hystrix-like, with hearing loss 0 trials

Including sub-types (0) Tagged with KID syndrome (0)

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