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Results 1 - 10 of 70 for Hearing problem
  1. SERAC1 gene 
    ... energy production and leading to the neurological and hearing problems characteristic of MEGDEL syndrome. It is unclear how ...
    https://medlineplus.gov/genetics/gene/serac1 - Genetics
  2. COL11A1 gene 
    ... and inner ear that lead to vision and hearing problems.In at least two reported cases, fibrochondrogenesis type ... condition include a distinctive facial appearance, eye abnormalities, hearing loss, and joint problems. These signs and symptoms tend to be less ...
    https://medlineplus.gov/genetics/gene/col11a1 - Genetics
  3. CACNA1D gene 
    ... slow and irregular heartbeat (bradycardia and arrhythmia) and hearing problems. These mutations likely impair the CaV1.3 channel's function in inner ear cells, impairing hearing, and in the cluster of cells in the ...
    https://medlineplus.gov/genetics/gene/cacna1d - Genetics
  4. COL11A2 gene 
    ... changes in the inner ear that lead to hearing problems. More About This Health Condition Mutations in the COL11A2 gene have been identified in people with nonsyndromic hearing loss, which is loss of hearing that is ...
    https://medlineplus.gov/genetics/gene/col11a2 - Genetics
  5. TWNK gene 
    ... unclear exactly how TWNK gene mutations lead to hearing problems and ovarian abnormalities in affected individuals. More About ...
    https://medlineplus.gov/genetics/gene/twnk - Genetics
  6. LARS2 gene 
    ... unclear exactly how LARS2 gene mutations lead to hearing problems and ovarian abnormalities in affected individuals. More About This Health Condition KIAA0028 leucine ... mitochondrial leucyl-tRNA synthetase, lead to premature ovarian failure and hearing loss in Perrault syndrome. Am J Hum Genet. ...
    https://medlineplus.gov/genetics/gene/lars2 - Genetics
  7. HARS2 gene 
    ... unclear exactly how HARS2 gene mutations lead to hearing problems and ovarian abnormalities in affected individuals. More About This Health Condition HARS-related ... synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndrome. Proc Natl Acad Sci ...
    https://medlineplus.gov/genetics/gene/hars2 - Genetics
  8. ATN1 gene 
    ... muscle tone (hypotonia), recurring seizures (epilepsy), vision and hearing problems, distinctive facial features, and skeletal abnormalities. Many affected ...
    https://medlineplus.gov/genetics/gene/atn1 - Genetics
  9. PEX1 gene 
    ... muscle tone (hypotonia), developmental delay, and vision and hearing problems. Mutations in the PEX1 gene are the most ...
    https://medlineplus.gov/genetics/gene/pex1 - Genetics
  10. FGFR2 gene 
    ... often have abnormalities of the fingers and toes, hearing and vision problems, and other signs and symptoms.More than 98 ... distinctive facial features. Affected individuals can have vision, hearing, and dental problems related to abnormal skull development. Most of the ...
    https://medlineplus.gov/genetics/gene/fgfr2 - Genetics
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