Deafness, Autosomal Recessive 39 (DFNB39)

Alias:

Dfnb39

Autosomal Recessive Nonsyndromic Deafness 39

Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 39

Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 39

Congenital Neurosensory Deafness Autosomal Recessive 39

Autosomal Recessive Nonsyndromic Hearing Loss 39

Deafness, Autosomal Recessive, Type 39

Deafness, Autosomal Recessive, 39

Autosomal Recessive Deafness 39

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Recessive 39, also known as dfnb39, is related to nonsyndromic hearing loss and deafness, autosomal recessive 24. An important gene associated with Deafness, Autosomal Recessive 39 is HGF (Hepatocyte Growth Factor), and among its related pathways/superpathways is Sensory processing of sound. Affiliated tissues include brain, and related phenotypes are prelingual sensorineural hearing impairment and nervous system

Related ID：

MALACARDS：DFN120

OMIM：608265

MESH：D006319