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Autosomal Recessive Nonsyndromic Hearing Loss 8 (MONDO:0010987)

An autosomal recessive nonsyndromic deafness that has material basis in mutation in the TMPRSS3 gene on chromosome 21q22.

Overview

Category

Ontology ID

Internal:12115

Synonyms

autosomal recessive nonsyndromic hearing loss 8

DFNB10

DFNB8

NRSD8

autosomal recessive deafness 10

autosomal recessive deafness 8

autosomal recessive nonsyndromic deafness 8

autosomal recessive nonsyndromic deafness type 8

childhood-onset neurosensory autosomal recessive deafness 8

deafness, autosomal recessive 10

deafness, autosomal recessive 8

deafness, autosomal recessive 8/10

deafness, autosomal recessive type 8

deafness, childhood-onset neurosensory, autosomal recessive 8

neurosensory nonsyndromic recessive deafness 8

Mapped terms

DOID:0110527

GARD:0022589

MEDGEN:322046

OMIM:601072

UMLS:C1832827

Child terms

Unknown children.