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Results 1 - 4 of 4 for "Deafness," autosomal "dominant," with peripheral neuropathy
  1. Nonsyndromic hearing loss 
    ... 2; DFNX2 DEAFNESS, X-LINKED 1; DFNX1 DEAFNESS, AUTOSOMAL DOMINANT 6; DFNA6 DEAFNESS, X-LINKED 5, WITH PERIPHERAL NEUROPATHY; DFNX5 DEAFNESS, AUTOSOMAL RECESSIVE 7; DFNB7 DEAFNESS, X- ...
    https://medlineplus.gov/genetics/condition/nonsyndromic-hearing-loss - Genetics
  2. OPA1 gene 
    ... a condition called optic atrophy type 1 and 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
  3. Hereditary sensory and autonomic neuropathy type IE 
    ... IE. DNMT1 ... disorder DNMT1-related dementia, deafness, and sensory neuropathy Hereditary sensory and autonomic neuropathy ...
    https://medlineplus.gov/...-sensory-and-autonomic-neuropathy-type-ie - Genetics
  4. 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