/autosomal dominant keratitis-ichthyosis-hearing loss syndrome

autosomal dominant keratitis-ichthyosis-hearing loss syndrome

Rare Disease

MONDO:0007850

Also Known As

KID syndrome, autosomal dominantautosomal dominant KID syndromekeratitis-ichthyosis -deafness syndromeautosomal dominant keratitis-ichthyosis-deafness syndromekeratitis-ichthyosis-deafness syndrome, autosomal dominant

Definition

Autosomal dominant form of KID syndrome.

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Associated Genes

GJB2 ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:148210 ↗

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