Deafness, Autosomal Dominant 78 (DFNA78)

Alias:

Dfna78

Deafness, Autosomal Dominant, Type 78

Hearing Loss, Autosomal Dominant 78

Deafness, Autosomal Dominant, 78

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 78, also known as dfna78, is related to autosomal dominant nonsyndromic deafness 78. An important gene associated with Deafness, Autosomal Dominant 78 is SLC12A2 (Solute Carrier Family 12 Member 2). Affiliated tissues include brain, and related phenotypes are macrocephaly and global developmental delay

Related ID：

MALACARDS：DFN385

OMIM：619081

MESH：D034381