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Results 1 - 5 of 5 for "Cone-rod" dystrophy hearing loss 2
  1. USH2A gene 
    ... Usher syndrome type IIA, while other mutations cause retinitis pigmentosa without hearing loss. More About This Health Condition US2 USH2 USH2A_ ...
    https://medlineplus.gov/genetics/gene/ush2a - Genetics
  2. MYO7A gene 
    ... some individuals who were thought to have nonsyndromic hearing loss developed retinitis pigmentosa (a vision disorder characteristic of Usher syndrome) later ...
    https://medlineplus.gov/genetics/gene/myo7a - Genetics
  3. RPGR gene 
    ... Clinical and immunohistochemical evidence for an X linked retinitis pigmentosa syndrome with recurrent infections and hearing loss in association with an RPGR mutation. J Med ...
    https://medlineplus.gov/genetics/gene/rpgr - Genetics
  4. CDH23 gene 
    ... development and function of stereocilia, which leads to hearing loss and difficulty with balance and coordination. A lack of this protein in the retina causes retinitis pigmentosa, a condition in which light-sensing cells of ...
    https://medlineplus.gov/genetics/gene/cdh23 - Genetics
  5. CLRN1 gene 
    ... III, which is characterized by a combination of hearing loss and vision loss. Some affected individuals also have ... This Health Condition MedlinePlus Genetics provides information about Retinitis pigmentosa More About This Health Condition USH3 USH3A USH3A_ ...
    https://medlineplus.gov/genetics/gene/clrn1 - Genetics