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Results 1 - 10 of 12 for Hearing "loss," autosomal dominant 77
  1. OPA1 gene 
    ... deafness, which results in both vision loss and hearing loss. OPA1 mutations can also cause a condition known as autosomal dominant optic atrophy (ADOA)-plus syndrome. ADOA-plus syndrome ...
    https://medlineplus.gov/genetics/gene/opa1 - 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. MYO7A 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 of ...
    https://medlineplus.gov/genetics/gene/myo7a - Genetics
  4. Craniofacial microsomia 
    ... report of nine familial cases with evidence of autosomal dominant inheritance and review of the literature. Clin Dysmorphol. 2009 Apr;18(2):67-77. doi: 10.1097/MCD.0b013e328323a7dd. Citation on PubMed ...
    https://medlineplus.gov/genetics/condition/craniofacial-microsomia - Genetics
  5. 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
  6. Osteopetrosis 
    ... are usually distinguished by their pattern of inheritance: autosomal dominant or autosomal recessive. The different types of the ... by the severity of their signs and symptoms.Autosomal dominant osteopetrosis (ADO), which is also called Albers-Schönberg ...
    https://medlineplus.gov/genetics/condition/osteopetrosis - Genetics
  7. Sotos syndrome 
    ... helped researchers determine that Sotos syndrome has an autosomal dominant pattern of inheritance. Autosomal dominant inheritance means one copy of the altered gene ...
    https://medlineplus.gov/genetics/condition/sotos-syndrome - Genetics
  8. 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
  9. Otospondylomegaepiphyseal dysplasia 
    ... spondylo-megaepiphyseal dysplasia Genetic Testing Registry: Otospondylomegaepiphyseal dysplasia, autosomal dominant Genetic Testing Registry: Otospondylomegaepiphyseal dysplasia, autosomal recessive Otospondylomegaepiphyseal ...
    https://medlineplus.gov/.../otospondylomegaepiphyseal-dysplasia - Genetics
  10. 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
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