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Autosomal Recessive Nonsyndromic Hearing Loss 32 (MONDO:0012091)

An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in variation in the chromosome region 1p22.1-p13.3.

Overview

Category

auditory system disorder

nervous system disorder

Ontology ID

MONDO:0012091

Internal:13157

Synonyms

CDC14A autosomal recessive nonsyndromic deafness

DFNB105

DFNB32

autosomal recessive deafness 105

autosomal recessive deafness 32

autosomal recessive nonsyndromic deafness 105

autosomal recessive nonsyndromic deafness 32

autosomal recessive nonsyndromic deafness caused by mutation in CDC14A

autosomal recessive nonsyndromic deafness type 105

autosomal recessive nonsyndromic deafness type 32

deafness, autosomal recessive 105

deafness, autosomal recessive 32

deafness, autosomal recessive 32, with or without immotile sperm

deafness, autosomal recessive type 105

Mapped terms

DOID:0110466

DOID:0110491

GARD:0022610

MEDGEN:373370

MESH:C563884

OMIM:608653

UMLS:C1837608

Child terms

Unknown children.

Results

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