Deafness, Autosomal Dominant 67 (DFNA67)

Alias:

Dfna67

Autosomal Dominant Nonsyndromic Deafness 67

Autosomal Dominant Nonsyndromic Hearing Loss 67

Deafness, Autosomal Dominant, Type 67

Deafness, Autosomal Dominant, 67

Autosomal Dominant Deafness 67

Favorite

Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 67, also known as dfna67, is related to deafness, autosomal dominant 68 and deafness, autosomal dominant 1, with or without thrombocytopenia. An important gene associated with Deafness, Autosomal Dominant 67 is OSBPL2 (Oxysterol Binding Protein Like 2). Affiliated tissues include brain, and related phenotypes are sensorineural hearing impairment and tinnitus

Related ID：

MALACARDS：DFN284

OMIM：616340

MESH：D006319