1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0080514 | Meier-Gorlin syndrome 3 | A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the ORC6 gene on chromosome 16q11. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| DOID:630 | genetic disease | A disease that has_material_basis_in genetic variations in the human genome. |
