| Term Name: | autosomal recessive nonsyndromic deafness 117 |
|---|---|
| Synonyms: | autosomal recessive deafness 117, DFNB117 |
| Definition: | An autosomal recessive nonsyndromic deafness characterized by bilateral moderate-to-profound sensorineural deafness with onset in early childhood that has_material_basis_in homozygous mutation in the CLRN2 gene on chromosome 4p15. |
| Ontology: | Human Disease [DOID:0070671] ( DOID:0070671 ) |