1 Child Term
Identifier | Name | Description |
---|---|---|
DOID:0070006 | Seckel syndrome 6 | A Seckel syndrome that has_material_basis_in homozygous mutation in the CEP63 gene on chromosome 3q22. |
1 Parent Term
Identifier | Name | Description |
---|---|---|
DOID:630 | genetic disease | A disease that has_material_basis_in genetic variations in the human genome. |