Warning: The NCBI web site requires JavaScript to function. more...

Full Report

Format

Full Report
Summary (Text)
Summary (XML)

Send to:

Choose Destination

File
Clipboard
Collections

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

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

Table of contents

Clinical resources

Molecular resources

Coriell Institute for Medical Research

Consumer resources

Reviews

Related information

MeSH
Related Medical Subject Headings
OMIM
Related records in OMIM
PMC Articles
Related information in PubMed Central Links
PubMed
Related literature resources in PubMed
PubMed (OMIM)
Related literature resources in PubMed

Recent activity

Clear Turn Off Turn On

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

MedGen

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...