| Term Name: | autosomal recessive nonsyndromic deafness 120 |
|---|---|
| Synonyms: | DFNB120 |
| Definition: | An autosomal recessive nonsyndromic deafness characterized by congenital or prelingual onset of severe to profound sensorineural hearing loss that has_material_basis_in homozygous mutation in the MINAR2 gene on chromosome 5q23. |
| Ontology: | Human Disease [DOID:0070674] ( DOID:0070674 ) |