Deafness, Autosomal Recessive 42 (DFNB42)

Alias:

Dfnb42

Autosomal Recessive Nonsyndromic Deafness 42

Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 42

Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 42

Congenital Neurosensory Deafness Autosomal Recessive 42

Autosomal Recessive Nonsyndromic Hearing Loss 42

Deafness, Autosomal Recessive, Type 42

Deafness, Autosomal Recessive, 42

Autosomal Recessive Deafness 42

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Recessive 42, also known as dfnb42, is related to deafness, autosomal recessive 21 and nonsyndromic hearing loss. An important gene associated with Deafness, Autosomal Recessive 42 is ILDR1 (Immunoglobulin Like Domain Containing Receptor 1), and among its related pathways/superpathways are Sensory processing of sound and Epithelial to mesenchymal transition in colorectal cancer. Affiliated tissues include brain, and related phenotypes are nervous system and hearing/vestibular/ear

Related ID：

MALACARDS：DFN244

OMIM：609646

MESH：D006319