| Metadata | |
|---|---|
| ID | 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 |
| Xrefs | |
| Synonyms |
autosomal recessive deafness 39 [EXACT] DFNB39 [EXACT] |
| Parent Relationships |