| Term Name: | autosomal recessive nonsyndromic deafness 79 |
|---|---|
| Synonyms: | autosomal recessive deafness 79, DFNB79 |
| Definition: | An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the TPRN gene on chromosome 9q34. |
| Ontology: | Human Disease [DOID:0110526] ( DOID:0110526 ) |