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Results 1 - 10 of 10 for Autosomal recessive nonsyndromic hearing loss 2
  1. GJB2 gene 
    ... and symptoms. Mutations in this gene can cause two forms of nonsyndromic hearing loss: DFNB1 and DFNA3.DFNB1 is inherited in an autosomal recessive pattern, which means both copies of the GJB2 ...
    https://medlineplus.gov/genetics/gene/gjb2 - Genetics
  2. TECTA gene 
    ... and symptoms. Mutations in this gene can cause two forms of nonsyndromic hearing loss: DFNA8/12 and DFNB21.DFNA8/12 is inherited in an autosomal dominant pattern, which means one mutated copy of ...
    https://medlineplus.gov/genetics/gene/tecta - Genetics
  3. COL11A2 gene 
    ... and symptoms. Mutations in this gene can cause two forms of nonsyndromic hearing loss: DFNA13 and DFNB53.DFNA13 is inherited in an autosomal dominant pattern, which means only one mutated copy ...
    https://medlineplus.gov/genetics/gene/col11a2 - Genetics
  4. MYO7A gene 
    ... Mutations in this gene are thought to cause two forms of nonsyndromic hearing loss: DFNA11 and DFNB2.DFNA11 is inherited in an autosomal dominant pattern, which means only one mutated copy ...
    https://medlineplus.gov/genetics/gene/myo7a - Genetics
  5. BSND gene 
    ... This Health Condition MedlinePlus Genetics provides information about Nonsyndromic hearing loss More About This ... PubMed BARTTIN CLCNK- ...
    https://medlineplus.gov/genetics/gene/bsnd - Genetics
  6. GJB3 gene 
    ... pathogenicity of GJB3 and GJB6 variants associated with nonsyndromic hearing loss. ... Non-syndromic, autosomal-recessive deafness. Clin Genet. 2006 May;69(5):371- ...
    https://medlineplus.gov/genetics/gene/gjb3 - Genetics
  7. CDH23 gene 
    ... Friedman TB, Morell RJ. Usher syndrome 1D and nonsyndromic autosomal ... features of hearing loss patients with CDH23 mutations: a large cohort study. ...
    https://medlineplus.gov/genetics/gene/cdh23 - Genetics
  8. STRC gene 
    ... on PubMed Redfield S, Shearer AE. STRC-Related Autosomal Recessive Hearing Loss. 2023 Dec 14. In: Adam MP, Feldman J, ...
    https://medlineplus.gov/genetics/gene/strc - Genetics
  9. GJA1 gene 
    ... This Health Condition MedlinePlus Genetics provides ... disorder are usually present in one of the two copies of the gene in each cell. Most ...
    https://medlineplus.gov/genetics/gene/gja1 - Genetics
  10. USH2A gene 
    ... mutations are the most common cause of the autosomal recessive form of retinitis pigmentosa, accounting for 10 to 15 percent of all cases. This form of the disorder is described as nonsyndromic, which means that it is not associated with ...
    https://medlineplus.gov/genetics/gene/ush2a - Genetics