1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0111434 | optic atrophy 10 | An optic atrophy characterized by early-onset optic neuropathy and mitochondrial defects that has_material_basis_in homozygous or compound heterozygous mutation in the RTN4IP1 gene on chromosome 6q21. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| DOID:5656 | cranial nerve disease | A neuropathy that is located_in one of the twelve cranial nerves. |
