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Autosomal Dominant Nonsyndromic Hearing Loss 53 (MONDO:0012380)

An autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 14q11.2-q12.

Overview

Category

Ontology ID

Internal:13431

Synonyms

DFNA53

autosomal dominant deafness 53

autosomal dominant nonsyndromic deafness 53

autosomal dominant nonsyndromic deafness type 53

deafness, autosomal dominant 53

deafness, autosomal dominant nonsyndromic sensorineural 53

Mapped terms

DOID:0110579

GARD:0009934

MEDGEN:355336

MESH:C566495

OMIM:609965

UMLS:C1864957

Child terms

Unknown children.