1 Child Term
Identifier | Name | Description |
---|---|---|
DOID:0110771 | hereditary spastic paraplegia 18 | A hereditary spastic paraplegia that has_material_basis_in mutation in the ERLIN2 gene on chromosome 8p11. |
1 Parent Term
Identifier | Name | Description |
---|---|---|
DOID:630 | genetic disease | A disease that has_material_basis_in genetic variations in the human genome. |