1 Child Term
Identifier | Name | Description |
---|---|---|
DOID:0111790 | congenital nystagmus 1 | A congenital nystagmus that has_material_basis_in mutation in the FRMD7 gene on chromosome Xq26.2. |
1 Parent Term
Identifier | Name | Description |
---|---|---|
DOID:5656 | cranial nerve disease | A neuropathy that is located_in one of the twelve cranial nerves. |