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Results 1 - 10 of 22 for Hearing "loss," autosomal dominant 80
  1. Nonsyndromic hearing loss 
    ... has different patterns of inheritance. Between 75 and 80 percent of cases ... has an autosomal dominant pattern of inheritance, which means one copy of ...
    https://medlineplus.gov/genetics/condition/nonsyndromic-hearing-loss - Genetics
  2. COL11A2 gene 
    ... 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 of ...
    https://medlineplus.gov/genetics/gene/col11a2 - Genetics
  3. DNMT1 gene 
    ... in people with a nervous system disorder called autosomal dominant cerebellar ataxia, deafness, and narcolepsy (ADCADN). Features of this disorder include difficulty coordinating movements (ataxia), hearing loss caused by abnormalities of the inner ear (sensorineural ...
    https://medlineplus.gov/genetics/gene/dnmt1 - Genetics
  4. LRP5 gene 
    ... These include autosomal dominant osteopetrosis type 1 and autosomal dominant osteosclerosis. In some cases, these conditions can cause abnormal bone growth and related skeletal abnormalities. Rarely, affected individuals have hearing loss or circulation problems in the brain. Other people ...
    https://medlineplus.gov/genetics/gene/lrp5 - Genetics
  5. Weissenbacher-Zweymüller syndrome 
    ... childhood. COL11A2 This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ... family. Heterozygous OSMED Heterozygous otospondylomegaepiphyseal ... fetal chondrodysplasia WZS Genetic ...
    https://medlineplus.gov/.../weissenbacher-zweymuller-syndrome - Genetics
  6. Stickler syndrome 
    ... I, II, and III are inherited in an autosomal dominant pattern, which means one copy of the altered ... their family.Marshall syndrome also typically has an autosomal dominant pattern of inheritance.Stickler syndrome types IV, V, ...
    https://medlineplus.gov/genetics/condition/stickler-syndrome - Genetics
  7. Diagnosed with NF2-Related Schwannomatosis (Children's Tumor Foundation) - PDF  
    Neurofibromatosis/Specifics ... Neurofibromatosis ... Children's Tumor Foundation ... PDF
    https://www.ctf.org/.../CTF-Diagnosed-with-NF2-Brochure-2024_v2.pdf - External Health Links
  8. Charcot-Marie-Tooth disease 
    ... and most intermediate forms are inherited in an autosomal dominant pattern. This pattern of inheritance means that one ... mild symptoms of the disorder.Some cases of autosomal dominant or type X Charcot-Marie-Tooth disease result ...
    https://medlineplus.gov/.../condition/charcot-marie-tooth-disease - Genetics
  9. Osteogenesis imperfecta 
    ... COL1A1 or COL1A2 gene, osteogenesis imperfecta has an autosomal dominant pattern of inheritance, which means one copy of ... gene. Type V is also inherited in an autosomal dominant pattern.Less commonly, osteogenesis imperfecta has an autosomal ...
    https://medlineplus.gov/genetics/condition/osteogenesis-imperfecta - Genetics
  10. Hereditary sensory and autonomic neuropathy type IE 
    ... IE. DNMT1 This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ... causes varied phenotypes of HSAN1 with dementia and hearing loss. Neurology. 2013 Feb 26;80(9):824-8. doi: 10.1212/WNL.0b013e318284076d. ...
    https://medlineplus.gov/...-sensory-and-autonomic-neuropathy-type-ie - Genetics
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