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Results 1 - 10 of 24 for Nonsyndromic hearing loss deafness
  1. Nonsyndromic hearing loss 
    ... inherited. Isolated deafness Nonsyndromic deafness Nonsyndromic hearing impairment Nonsyndromic hearing loss and deafness Genetic Testing Registry: Nonsyndromic genetic hearing loss Genetic ...
    https://medlineplus.gov/genetics/condition/nonsyndromic-hearing-loss - Genetics
  2. MT-TS1 gene 
    ... 27. Citation on PubMed Usami SI, Nishio SY. Nonsyndromic Hearing Loss and Deafness, Mitochondrial. 2004 Oct 22 [updated 2018 Jun 14]. ...
    https://medlineplus.gov/genetics/gene/mt-ts1 - Genetics
  3. GJB2 gene 
    ... NBK1272/ Citation on PubMed Smith RJH, Ranum PT. Nonsyndromic Hearing Loss and Deafness, DFNA3 - RETIRED CHAPTER, FOR HISTORICAL REFERENCE ONLY. 1998 ...
    https://medlineplus.gov/genetics/gene/gjb2 - Genetics
  4. GJB6 gene 
    ... 0b013e32830e20b0. Citation on PubMed Smith RJH, Ranum PT. Nonsyndromic Hearing Loss and Deafness, DFNA3 - RETIRED CHAPTER, FOR HISTORICAL REFERENCE ONLY. 1998 ...
    https://medlineplus.gov/genetics/gene/gjb6 - Genetics
  5. Palmoplantar keratoderma with deafness 
    ... Marlin S. The GJB2 mutation R75Q can cause nonsyndromic hearing loss DFNA3 or hereditary palmoplantar keratoderma with deafness. Am J Med Genet A. 2005 Aug 30; ...
    https://medlineplus.gov/.../palmoplantar-keratoderma-with-deafness - Genetics
  6. NIDCD Glossary From the National Institutes of Health (National Institute on Deafness and Other Communication Disorders)  
    Ear Infections/Reference Desk ... Ear Infections ... Dizziness and Vertigo/Reference Desk ... Dizziness and Vertigo ... Hearing Disorders and Deafness/Reference Desk ... Hearing ...
    https://www.nidcd.nih.gov/glossary - External Health Links
  7. POU3F4 gene 
    ... designated as DFNX2, sometimes also known as Nance deafness. DFNX2 is the most common type of X-linked nonsyndromic hearing loss, accounting for about half of all cases. X- ...
    https://medlineplus.gov/genetics/gene/pou3f4 - Genetics
  8. BSND gene 
    ... This Health Condition MedlinePlus Genetics provides information about Nonsyndromic hearing loss More About This Health Condition BART Bartter syndrome, infantile, with sensorineural deafness (Barttin) barttin barttin CLCNK-type chloride channel accessory ...
    https://medlineplus.gov/genetics/gene/bsnd - Genetics
  9. WFS1 gene 
    ... loss called DFNA6. People with this condition have hearing loss without related signs and symptoms affecting other parts of the body. Individuals with DFNA6 nonsyndromic deafness cannot hear low tones (low-frequency sounds), such ...
    https://medlineplus.gov/genetics/gene/wfs1 - Genetics
  10. ACTG1 gene 
    ... This Health Condition MedlinePlus Genetics provides information about ... protein cytoskeletal gamma-actin deafness, autosomal dominant 20 deafness, autosomal dominant 26 DFNA20 ...
    https://medlineplus.gov/genetics/gene/actg1 - Genetics
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