1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0110509 | autosomal recessive nonsyndromic deafness 53 | 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 COL11A2 gene on chromosome 6p21. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| DOID:2742 | auditory system disease | A sensory system disease that is characterized by auditory dysfunction located_in the auditory system. |
