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Results 1 - 10 of 43 for Inner ear disorder
  1. DNMT1 gene 
    ... ataxia), hearing loss caused by abnormalities of the inner ear (sensorineural deafness), and excessive daytime sleepiness (narcolepsy). Cognitive decline occurs as the disorder progresses. Numbness, tingling, or pain in the arms ...
    https://medlineplus.gov/genetics/gene/dnmt1 - Genetics
  2. CLCNKB gene 
    ... that is also found in the kidneys and inner ear. A combination of CLCNKA and CLCNKB gene mutations causes a life-threatening form of the disorder known as Bartter syndrome type IV or antenatal ...
    https://medlineplus.gov/genetics/gene/clcnkb - Genetics
  3. CLCNKA gene 
    ... that is also found in the kidneys and inner ear. A combination of CLCNKA and CLCNKB gene mutations causes a life-threatening form of the disorder called Bartter syndrome type IV. This condition is ...
    https://medlineplus.gov/genetics/gene/clcnka - Genetics
  4. ATP6V0A4 gene 
    ... the proper pH of the fluid in the inner ear (endolymph). Several ATP6V0A4 gene mutations have been identified in people with renal tubular acidosis with deafness, a disorder involving excess acid in the blood (metabolic acidosis), ...
    https://medlineplus.gov/genetics/gene/atp6v0a4 - Genetics
  5. NDP gene 
    ... blood vessels in the retina and in the inner ear. Several NDP gene variants (also called mutations) have been found to cause the eye disorder familial exudative vitreoretinopathy. This disorder affects the retina ...
    https://medlineplus.gov/genetics/gene/ndp - Genetics
  6. ATP6V1B1 gene 
    ... the proper pH of the fluid in the inner ear (endolymph). More than 25 ATP6V1B1 gene mutations have been identified in people with renal tubular acidosis with deafness, a disorder involving excess acid in the blood (metabolic acidosis), ...
    https://medlineplus.gov/genetics/gene/atp6v1b1 - Genetics
  7. FZD4 gene 
    ... blood vessels in the retina and in the inner ear. Variants (also called mutations) in the FZD4 gene have been identified in people with an eye disorder called familial exudative vitreoretinopathy. This disorder affects the ...
    https://medlineplus.gov/genetics/gene/fzd4 - Genetics
  8. RERE gene 
    ... role in the development of the brain, eyes, inner ear, heart, and kidneys. More than 15 mutations in the RERE gene have been found to cause a condition called neurodevelopmental disorder with or without anomalies of the brain, eye, ...
    https://medlineplus.gov/genetics/gene/rere - Genetics
  9. EDNRB gene 
    ... also involved in the normal function of the inner ear. Variants (also known as mutations) in the EDNRB gene have been found to cause Hirschsprung disease, a disorder that causes severe constipation or blockage of the ...
    https://medlineplus.gov/genetics/gene/ednrb - Genetics
  10. EDN3 gene 
    ... also involved in the normal function of the inner ear. Variants (also known as mutations) in the EDN3 gene have been found to cause Hirschsprung disease, a disorder that causes severe constipation or blockage of the ...
    https://medlineplus.gov/genetics/gene/edn3 - Genetics
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