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Results 1 - 10 of 16 for "Deafness," autosomal recessive 21
  1. Nonsyndromic hearing loss 
    ... DOMINANT 20; DFNA20 DEAFNESS, AUTOSOMAL DOMINANT 23; DFNA23 DEAFNESS, AUTOSOMAL RECESSIVE 21; DFNB21 DEAFNESS, AUTOSOMAL RECESSIVE 13; DFNB13 DEAFNESS, AUTOSOMAL ...
    https://medlineplus.gov/genetics/condition/nonsyndromic-hearing-loss - Genetics
  2. CDH23 gene 
    ... TB, Morell RJ. Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23. Am J Hum Genet. 2001 Jan;68(1):26-37. doi: 10.1086/316954. Epub 2000 Nov 21. Citation on PubMed or Free article on PubMed ...
    https://medlineplus.gov/genetics/gene/cdh23 - Genetics
  3. STRC gene 
    ... deafness-infertility syndrome. More About This Health Condition deafness, autosomal recessive 16 DFNB16 STRC_HUMAN Tests of STRC PubMed ...
    https://medlineplus.gov/genetics/gene/strc - Genetics
  4. GJB3 gene 
    ... on PubMed Petersen MB, Willems PJ. Non-syndromic, autosomal-recessive deafness. Clin Genet. 2006 May;69(5):371-92. ...
    https://medlineplus.gov/genetics/gene/gjb3 - Genetics
  5. TECTA gene 
    ... alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21. Hum Mol Genet. 1999 Mar;8(3): ...
    https://medlineplus.gov/genetics/gene/tecta - Genetics
  6. SLC26A4 gene 
    ... ER. A mutation in PDS causes non-syndromic recessive deafness. Nat Genet. 1998 ... protein. Nat Genet. 1999 Apr;21(4):440-3. doi: 10.1038/7783. Citation ...
    https://medlineplus.gov/genetics/gene/slc26a4 - Genetics
  7. Wolfram syndrome 
    ... the CISD2 gene is also inherited in an autosomal recessive pattern. Diabetes insipidus and mellitus with optic atrophy and deafness Diabetes insipidus, diabetes mellitus, optic atrophy, and deafness ...
    https://medlineplus.gov/genetics/condition/wolfram-syndrome - Genetics
  8. Craniometaphyseal dysplasia 
    ... activity. J Biol Chem. 2007 May 25;282(21):15872-83. doi: ... recessive GJA1 missense mutation linked to Craniometaphyseal dysplasia. PLoS ...
    https://medlineplus.gov/.../condition/craniometaphyseal-dysplasia - Genetics
  9. Congenital deafness with labyrinthine aplasia, microtia, and microdontia 
    ... mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show signs and symptoms of the condition. Congenital deafness with inner ear agenesis, microtia, and microdontia Deafness ...
    https://medlineplus.gov/...rinthine-aplasia-microtia-and-microdontia - Genetics
  10. Björnstad syndrome 
    ... mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show signs and symptoms of the condition. Bjornstad syndrome BJS Deafness and pili torti, Bjornstad type Pili torti and ...
    https://medlineplus.gov/genetics/condition/bjornstad-syndrome - Genetics
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