Keratitis-Ichthyosis-Deafness Syndrome, Autosomal Dominant (KIDAD)

Alias:

Keratitis-Ichthyosis-Deafness Syndrome

Autosomal Dominant Keratitis-Ichthyosis-Deafness Syndrome

Keratitis Ichthyosis and Deafness Syndrome

Kid Syndrome

Kidad

Ichthyosiform Erythroderma, Corneal Involvement, and Deafness

Autosomal Dominant Keratitis-Ichthyosis-Hearing Loss Syndrome

Keratitis, Ichthyosis, and Deafness

Kid Syndrome, Autosomal Dominant

Autosomal Dominant Kid Syndrome

Senter Syndrome

Favorite

Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Keratitis-Ichthyosis-Deafness Syndrome, Autosomal Dominant, also known as keratitis-ichthyosis-deafness syndrome, is related to ichthyosis and skin disease, and has symptoms including photophobia An important gene associated with Keratitis-Ichthyosis-Deafness Syndrome, Autosomal Dominant is GJB2 (Gap Junction Protein Beta 2). Affiliated tissues include skin and eye, and related phenotypes are sensorineural hearing impairment and ichthyosis

Related ID：

MALACARDS：KRT028

OMIM：148210

MESH：D003638