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Results 1 - 6 of 6 for Hearing "loss," autosomal dominant 79
  1. WFS1 gene 
    ... Kunst HP, Hoefsloot EH, Cruysberg JR, Cremers CW. Autosomal dominant optic neuropathy and sensorineual hearing loss associated with a novel mutation of WFS1. Mol ...
    https://medlineplus.gov/genetics/gene/wfs1 - Genetics
  2. Stickler syndrome 
    ... Van de Heyning P, Usami S. A new autosomal recessive form of Stickler syndrome is caused by a mutation in the COL9A1 gene. Am J Hum Genet. 2006 Sep;79(3):449-57. doi: 10.1086/506478. Epub 2006 Jun 26. Citation on PubMed or Free article on PubMed Central
    https://medlineplus.gov/genetics/condition/stickler-syndrome - Genetics
  3. Spondyloepiphyseal dysplasia congenita 
    ... Fabre A, Genevieve D, Touitou I. Confirmation of autosomal recessive inheritance ... J. 2000 Mar;79(3):178-82. Citation on PubMed Gregersen PA, ...
    https://medlineplus.gov/.../spondyloepiphyseal-dysplasia-congenita - Genetics
  4. Kniest dysplasia 
    ... dysplasia. COL2A1 Kniest dysplasia is inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/genetics/condition/kniest-dysplasia - Genetics
  5. Spinocerebellar ataxia type 36 
    ... SCA36. NOP56 This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-36 - Genetics
  6. Saethre-Chotzen syndrome 
    ... chromosome 7 This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/genetics/condition/saethre-chotzen-syndrome - Genetics