KID syndrome

rare

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.

Identifiers: MONDO:0018781 Orphanet:477
Part of: Diffuse palmoplantar keratoderma Ectodermal dysplasia syndrome
Also known as: ichthyosis hystrix Rheydt type · Keratitis Ichthyosis Deafness Syndrome · keratitis, ichthyosis, and deafness (KID) syndrome · keratitis-ichthyosis-deafness/Hystrix-like ichthyosis-deafness syndrome · KID/HID syndrome

Subtypes

All diseases Rare only

Disease	ID	Genes
Autosomal dominant keratitis-ichthyosis-hearing loss syndrome	MONDO:0007850
Ichthyosiform erythroderma, corneal involvement, and hearing loss	MONDO:0009440	AP1B1
Ichthyosis, hystrix-like, with hearing loss	MONDO:0011245

Projects

Including projects on subtypes.

No projects yet.