1 Child Term
Identifier | Name | Description |
---|---|---|
DOID:0111031 | hemochromatosis type 5 | A hemochromatosis that has_material_basis_in heterozygous mutation in the FTH1 gene on chromosome 11q12. |
1 Parent Term
Identifier | Name | Description |
---|---|---|
DOID:630 | genetic disease | A disease that has_material_basis_in genetic variations in the human genome. |