1 Child Term
Identifier | Name | Description |
---|---|---|
DOID:0110495 | autosomal recessive nonsyndromic deafness 37 | An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has_material_basis_in mutation in the MYO6 gene on chromosome 6q14. |
1 Parent Term
Identifier | Name | Description |
---|---|---|
DOID:863 | nervous system disease | A disease of anatomical entity that is located_in the central nervous system or located_in the peripheral nervous system. |