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Autosomal dominant nonsyndromic hearing loss 18(DFNA18)

MedGen UID:: 340051
•Concept ID:: C1853760
•: Disease or Syndrome

Synonym:	Deafness, autosomal dominant 18

Monarch Initiative:	MONDO:0011625
OMIM®:	606012

Definition

An autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 3q22. [from MONDO]

Clinical features

From HPO

Progressive hearing impairment

MedGen UID:: 331224
•Concept ID:: C1842138
•: Finding

A progressive form of hearing impairment.

See: Feature record | Search on this feature

Ear malformation
- Progressive hearing impairment

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVHereditary hearing loss and deafness

Hereditary hearing loss and deafness
- Nonsyndromic genetic hearing loss
  - Autosomal dominant nonsyndromic hearing loss
    - Autosomal dominant nonsyndromic hearing loss 18

Supplemental Content

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Clinical resources

Molecular resources

Coriell Institute for Medical Research

Consumer resources

Reviews

Related information

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Autosomal dominant nonsyndromic hearing loss 18
Autosomal dominant nonsyndromic hearing loss 18

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