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Results 1 - 9 of 9 for Hearing "loss," autosomal dominant 88
  1. Dentinogenesis imperfecta 
    ... whether DSPP gene mutations are related to the hearing loss found in a few older individuals with dentinogenesis imperfecta type II. DSPP This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/genetics/condition/dentinogenesis-imperfecta - Genetics
  2. GJB3 gene 
    ... encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment. Nat Genet. 1998 Dec;20(4): ...
    https://medlineplus.gov/genetics/gene/gjb3 - Genetics
  3. Cornelia de Lange syndrome 
    ... gene, the condition is considered to have an autosomal dominant pattern of inheritance. Autosomal dominant inheritance means one copy of the altered gene ...
    https://medlineplus.gov/.../condition/cornelia-de-lange-syndrome - Genetics
  4. Hereditary paraganglioma-pheochromocytoma 
    ... SDHD Hereditary paraganglioma-pheochromocytoma is inherited in an autosomal dominant pattern, which means one copy of the altered ... Niemann S, Muller U. Mutations in SDHC cause autosomal dominant paraganglioma, type 3. Nat Genet. 2000 Nov;26( ...
    https://medlineplus.gov/...hereditary-paraganglioma-pheochromocytoma - Genetics
  5. Physical Therapy for Facioscapulohumeral Muscular Dystrophy (FSHD) (FacioScapuloHumeral Muscular Dystrophy Society) - PDF  
    Muscular Dystrophy/Living With ... Muscular Dystrophy ... FacioScapuloHumeral Muscular Dystrophy Society ... PDF
    https://www.fshdsociety.org/.../FSH-Society-PT-for-FSHD-Brochure.pdf - External Health Links
  6. Multiple familial trichoepithelioma 
    ... CYLD Susceptibility to multiple familial trichoepithelioma has an autosomal dominant pattern of inheritance, which means one copy of ...
    https://medlineplus.gov/.../multiple-familial-trichoepithelioma - Genetics
  7. Distal 18q deletion syndrome 
    ... 18q deletion syndrome is considered to be an autosomal dominant condition, which means one copy of the deleted ...
    https://medlineplus.gov/.../condition/distal-18q-deletion-syndrome - Genetics
  8. COL2A1 gene 
    ... JJ, van Driel MA, Cremers FP, Hoyng CB. Autosomal dominant rhegmatogenous retinal detachment associated with an Arg453Ter mutation ...
    https://medlineplus.gov/genetics/gene/col2a1 - Genetics
  9. Apert syndrome 
    ... feet. FGFR2 Apert syndrome is inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/genetics/condition/apert-syndrome - Genetics