1. Mendelian
  2. Rare Disease Genes
  3. SLC44A4

SLC44A4 gene related symptoms and diseases

All the information presented here about the SLC44A4 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,NCBIGENE,OMIM,ORPHANET, Mendelian Rare Disease Search Engine.

Table of contents:

Top 5 symptoms and clinical features associated to SLC44A4 gene

Symptoms // Phenotype % Cases
Hearing impairment Uncommon - Between 30% and 50% cases
Sensorineural hearing impairment Uncommon - Between 30% and 50% cases
Vertigo Uncommon - Between 30% and 50% cases
Progressive hearing impairment Uncommon - Between 30% and 50% cases
Tinnitus Uncommon - Between 30% and 50% cases

Rare diseases associated to SLC44A4 gene

Here you will find a list of rare diseases related to the SLC44A4. You can also use our tool to get a more accurate diagnosis based on your current symptoms.


DEAFNESS, AUTOSOMAL DOMINANT 72; DFNA72

Most common symptoms of DEAFNESS, AUTOSOMAL DOMINANT 72; DFNA72

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


More info about DEAFNESS, AUTOSOMAL DOMINANT 72; DFNA72

SOURCES: OMIM

AUTOSOMAL DOMINANT NON-SYNDROMIC SENSORINEURAL DEAFNESS TYPE DFNA

Alternate names

AUTOSOMAL DOMINANT NON-SYNDROMIC SENSORINEURAL DEAFNESS TYPE DFNA Is also known as autosomal dominant non-syndromic sensorineural hearing loss type dfna, autosomal dominant isolated sensorineural deafness type dfna, autosomal dominant isolated sensorineural hearing loss type dfna, autosomal dominant isolated neurosensory deafness type dfna


More info about AUTOSOMAL DOMINANT NON-SYNDROMIC SENSORINEURAL DEAFNESS TYPE DFNA

SOURCES: ORPHANET


Potential gene panels for SLC44A4 gene

SLC44A4 Panel

United States.

By Fulgent Genetics Fulgent Genetics

This panel specifically test the SLC44A4 gene.

More info about this panel
United States.

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