Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 6 of 6 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. Adult Refsum disease From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Leukodystrophies/Specifics ... Leukodystrophies ... Leukodystrophy refers to genetic diseases that predominantly affect the white matter of the central nervous ...
    https://www.ninds.nih.gov/.../leukodystrophy#refsum-disease-adult - External Health Links
  5. Leukodystrophy From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Leukodystrophies/Start Here ... Leukodystrophies ... National Institute of Neurological Disorders and Stroke ... From the National Institutes of Health ... Leukodystrophy ...
    https://www.ninds.nih.gov/.../disorders/leukodystrophy - External Health Links
  6. 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