autosomal recessive nonsyndromic deafness 39

Term ID

DOID:0110497

Synonyms

• autosomal recessive deafness 39
• DFNB39

Definition

An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, downsloping hearing loss and has_material_basis_in mutation in the HGF gene on chromosome 7q21. https://www.ncbi.nlm.nih.gov/pubmed/19576567

References

• ICD10CM:H90.3
• OMIM:608265

Ontology

Human Disease   ( DOID:0110497 )