Terminology Service for NFDI4Health
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Deafness, Autosomal Recessive 39

Go to external page http://purl.obolibrary.org/obo/NCIT_C129874

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

Term info

Label

Deafness, Autosomal Recessive 39

Synonyms
  • DFNB39
  • Deafness, Autosomal Recessive 39
Preferred Name

Deafness, Autosomal Recessive 39

Semantic Type

Disease or Syndrome

UMLS CUI

C1842342

code

C129874