| Term Name: | autosomal recessive nonsyndromic deafness 23 |
|---|---|
| Synonyms: | autosomal recessive deafness 23, DFNB23 |
| 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 PCDH15 gene on chromosome 10q21. |
| Ontology: | Human Disease [DOID:0110481] ( DOID:0110481 ) |