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autosomal dominant keratitis-ichthyosis-deafness syndrome

Disease Summary
Associated Targets (1)


Mondo Description Autosomal dominant form of KID syndrome.
Uniprot Description An autosomal dominant form of ectodermal dysplasia. Ectodermal dysplasia defines a heterogeneous group of disorders due to abnormal development of two or more ectodermal structures. Keratitis-ichthyosis-deafness syndrome is characterized by the association of hyperkeratotic skin lesions with vascularizing keratitis and profound sensorineural hearing loss. Clinical features include deafness, ichthyosis, photophobia, absent or decreased eyebrows, sparse or absent scalp hair, decreased sweating and dysplastic finger and toenails.
Mondo Term and Equivalent IDs
MONDO:0007850:  autosomal dominant keratitis-ichthyosis-deafness syndrome