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Autosomal Recessive Nonsyndromic Hearing Loss 39 (MONDO:0012003)

An autosomal recessive disorder caused by mutations in the HGF gene, encoding hepatocyte growth factor receptor. It is characterized by profound deafness.

Overview

Category

auditory system disorder

nervous system disorder

Ontology ID

MONDO:0012003

Internal:13074

Synonyms

autosomal recessive nonsyndromic hearing loss 39

DFNB39

HGF autosomal recessive nonsyndromic deafness

autosomal recessive deafness 39

autosomal recessive nonsyndromic deafness 39

autosomal recessive nonsyndromic deafness caused by mutation in HGF

autosomal recessive nonsyndromic deafness type 39

deafness, autosomal recessive 39

deafness, autosomal recessive type 39

Mapped terms

DOID:0110497

GARD:0022608

MEDGEN:374909

MESH:C564265

NCIT:C129874

OMIM:608265

UMLS:C1842342

Child terms

Unknown children.

Results

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