Autosomal dominant keratitis-ichthyosis-hearing loss syndrome

MONDO:0007850

Autosomal dominant form of KID syndrome.

Also known as: KID syndrome, autosomal dominant, keratitis-ichthyosis -deafness syndrome, autosomal dominant keratitis-ichthyosis-deafness syndrome, keratitis-ichthyosis-deafness syndrome, autosomal dominant

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Broader categories

Disease (680) Hereditary disease (176) Skin disorder (132) Syndromic disease (25) Human disease (14) Hereditary skin disorder (6) Keratosis (4) Palmoplantar keratosis (4) Ectodermal dysplasia syndrome (3) Disease of genetic or genomic mechanism (2)

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