| Term Name: | autosomal recessive nonsyndromic deafness 31 |
|---|---|
| Synonyms: | autosomal recessive deafness 31, DFNB31 |
| Definition: | An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has_material_basis_in mutation in the WHRN gene on chromosome 9q32. |
| Ontology: | Human Disease [DOID:0110490] ( DOID:0110490 ) |