Deafness, Autosomal Recessive 97 (DFNB97)

Alias:

Dfnb97

Autosomal Recessive Nonsyndromic Deafness 97

Autosomal Recessive Nonsyndromic Hearing Loss 97

Deafness, Autosomal Recessive, Type 97

Deafness, Autosomal Recessive, 97

Autosomal Recessive Deafness 97

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Recessive 97, also known as dfnb97, is related to familial renal papillary carcinoma and mucinous bronchioloalveolar adenocarcinoma. An important gene associated with Deafness, Autosomal Recessive 97 is MET (MET Proto-Oncogene, Receptor Tyrosine Kinase), and among its related pathways/superpathways are Signal Transduction and RAF/MAP kinase cascade. Affiliated tissues include brain, and related phenotypes are sensorineural hearing impairment and Increased shRNA abundance (Z-score > 2)

Related ID：

MALACARDS：DFN330

OMIM：616705

MESH：D006319