Deafness, Autosomal Recessive 98 (DFNB98)

Alias:

Dfnb98

Autosomal Recessive Nonsyndromic Deafness 98

Autosomal Recessive Nonsyndromic Hearing Loss 98

Deafness, Autosomal Recessive, Type 98

Deafness, Autosomal Recessive, 98

Autosomal Recessive Deafness 98

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Recessive 98, also known as dfnb98, is related to tooth agenesis, selective, 10 and deafness, autosomal recessive 8. An important gene associated with Deafness, Autosomal Recessive 98 is TSPEAR (Thrombospondin Type Laminin G Domain And EAR Repeats), and among its related pathways/superpathways are Cardiac conduction and Endometrial cancer. Affiliated tissues include brain, and related phenotypes are sensorineural hearing impairment and hearing/vestibular/ear

Related ID：

MALACARDS：DFN269

OMIM：614861

MESH：D006319