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Autosomal Recessive Nonsyndromic Hearing Loss 46 (MONDO:0012327)

An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 18p11.32-p11.31.

Overview

Category

Ontology ID

Internal:13383

Synonyms

DFNB46

autosomal recessive deafness 46

autosomal recessive nonsyndromic deafness 46

autosomal recessive nonsyndromic deafness type 46

deafness, autosomal recessive 46

Mapped terms

DOID:0110503

GARD:0022615

MEDGEN:355302

MESH:C566459

OMIM:609647

UMLS:C1864815

Child terms

Unknown children.