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DFNA 3 Nonsyndromic Hearing Loss and Deafness(DFNA3)

MedGen UID:: 431596
•Concept ID:: CN043589
•: Disease or Syndrome

Synonym:	DFNA3

Related genes: Gene(s) associated with related conditions. For conditions in a hierarchy, the parent condition will list the genes associated with the children conditions.	GJB6, GJB2

Definition

Nonsyndromic hearing loss and deafness, DFNA3 is characterized by pre- or postlingual mild-to-profound progressive high-frequency sensorineural hearing impairment. Affected individuals have no other associated medical findings. [from GeneReviews]

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVDFNA 3 Nonsyndromic Hearing Loss and Deafness
- CROGVAutosomal dominant nonsyndromic hearing loss 3A
- CROGVAutosomal dominant nonsyndromic hearing loss 3B

DFNA 3 Nonsyndromic Hearing Loss and Deafness
- Autosomal dominant nonsyndromic hearing loss 3A
- Autosomal dominant nonsyndromic hearing loss 3B

Supplemental Content

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Genetic Testing Registry

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ClinicalTrials.gov

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MedlinePlus

Reviews

Related information

GTR
Related information in GTR
GTR(Clinical)
Clinical tests in GTR
PMC Articles
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