U.S. flag

An official website of the United States government


Send to:

Choose Destination

Autosomal recessive nonsyndromic hearing loss 18A(DFNB18; DFNB18A)

MedGen UID:
Concept ID:
Disease or Syndrome
Synonyms: Deafness, autosomal recessive 18; Deafness, autosomal recessive 18A; DFNB18 Nonsyndromic Hearing Loss and Deafness
Gene (location): USH1C (11p15.1)
Monarch Initiative: MONDO:0011192
OMIM®: 602092


Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the USH1C gene. [from MONDO]

Clinical features

From HPO
Sensorineural hearing impairment
MedGen UID:
Concept ID:
Disease or Syndrome
A type of hearing impairment in one or both ears related to an abnormal functionality of the cochlear nerve.

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  

Supplemental Content

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...