1. Mendelian
  2. Rare Diseases
  3. DEAFNESS, AUTOSOMAL DOMINANT 72; DFNA72

Deafness, Autosomal Dominant 72; Dfna72

Table of contents:

Genes related to Deafness, Autosomal Dominant 72; Dfna72

  • SLC44A4

View recommended genes panels

Clinical Features

Phenotypes and symptoms related to Deafness, Autosomal Dominant 72; Dfna72

  • Hearing impairment
  • Sensorineural hearing impairment
  • Vertigo
  • Progressive hearing impairment
  • Tinnitus

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— No data available about the known clinical features onset.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Deafness, Autosomal Dominant 72; Dfna72 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
SLC44A4.

By Fulgent Genetics Fulgent Genetics (United States).

SLC44A4
Specificity
100 %
Genes
100 %

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Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Search Engine

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