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Results 1 - 10 of 17 for Sensorineural hearing loss disorder
  1. ATP6V0A4 gene 
    ... loss caused by changes in the inner ear (sensorineural hearing loss).Mutations in the ATP6V0A4 gene impair the function ... the inner ear is also impaired, resulting in sensorineural hearing loss. More About This Health Condition ATP6V0A4 gene mutations ...
    https://medlineplus.gov/genetics/gene/atp6v0a4 - Genetics
  2. ATP6V1B1 gene 
    ... loss caused by changes in the inner ear (sensorineural hearing loss).Mutations in the ATP6V1B1 gene impair the function ... the inner ear is also impaired, resulting in sensorineural hearing loss. More About This Health Condition ATP6B1 ATPase, H+ ...
    https://medlineplus.gov/genetics/gene/atp6v1b1 - Genetics
  3. WFS1 gene 
    ... WFS1) are a common cause of low frequency sensorineural hearing loss. Hum Mol Genet. 2001 Oct 15;10(22): ... in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations. Hum Genet. 2002 ...
    https://medlineplus.gov/genetics/gene/wfs1 - Genetics
  4. RRM2B gene 
    ... loss caused by problems with the inner ear (sensorineural hearing loss), and digestive problems.Typically, mutations that cause progressive ...
    https://medlineplus.gov/genetics/gene/rrm2b - Genetics
  5. KCNQ4 gene 
    ... and conductance of the KCNQ4 channel lead to sensorineural hearing loss. J Cell Mol Med. 2013 Jul;17(7): ...
    https://medlineplus.gov/genetics/gene/kcnq4 - Genetics
  6. ATP1A3 gene 
    ... cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss. This specific presentation is known as CAPOS syndrome ( ...
    https://medlineplus.gov/genetics/gene/atp1a3 - Genetics
  7. PRPS1 gene 
    ... hearing caused by changes in the inner ear (sensorineural hearing loss), weak muscle tone (hypotonia), impaired muscle coordination (ataxia), ...
    https://medlineplus.gov/genetics/gene/prps1 - Genetics
  8. HARS2 gene 
    ... histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndrome. Proc Natl Acad Sci U ...
    https://medlineplus.gov/genetics/gene/hars2 - Genetics
  9. CLCNKA gene 
    ... is also known as antenatal Bartter syndrome with sensorineural deafness because affected individuals have hearing loss caused by abnormalities in the inner ear.Mutations ...
    https://medlineplus.gov/genetics/gene/clcnka - Genetics
  10. CLCNKB gene 
    ... syndrome type IV or antenatal Bartter syndrome with sensorineural deafness. In addition to salt wasting, this form of the disorder is characterized by hearing loss that results from a loss of ClC-Ka ...
    https://medlineplus.gov/genetics/gene/clcnkb - Genetics
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