| Term Name: | autosomal recessive nonsyndromic deafness 30 |
|---|---|
| Synonyms: | autosomal recessive deafness 30, DFNB30 |
| Definition: | An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutations in the MYO3A gene on chromosome 10p12.1. |
| Ontology: | Human Disease [DOID:0110489] ( DOID:0110489 ) |