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Autosomal Recessive Nonsyndromic Hearing Loss 40 (MONDO:0012002)

An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 22q11.21-q12.1.

Overview

Category

Ontology ID

Internal:13073

Synonyms

DFNB40

autosomal recessive deafness 40

autosomal recessive nonsyndromic deafness 40

autosomal recessive nonsyndromic deafness type 40

deafness, autosomal recessive 40

Mapped terms

DOID:0110499

GARD:0022607

MEDGEN:334053

MESH:C564266

OMIM:608264

UMLS:C1842345

Child terms

Unknown children.