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Metadata
DOID DOID:0110497
Name autosomal recessive nonsyndromic deafness 39
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
Synonyms

autosomal recessive deafness 39 [EXACT]

DFNB39 [EXACT]

Xrefs

ICD10CM:H90.3

OMIM:608265

Relationships

is_a autosomal recessive nonsyndromic deafness

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