1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0070260 | congenital disorder of glycosylation type IIh | A congenital disorder of glycosylation type II that has_material_basis_in a mutation of the COG8 gene on chromosome 16q22.1. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0014667 | disease of metabolism | A disease that involving errors in metabolic processes of building or degradation of molecules. |
