Hemochromatosis Type 1
Disease ID: disease_node_17559
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| Dbxref | GARD:10417, ICD10CM:E83.1, MIM:235200, ORDO:465508 |
|---|---|
| Subclassof | DOID_2352 |
| Data Source | DOID |
| Synonyms | HFE1, symptomatic form of HFE-related hereditary hemochromatosis, symptomatic form of classic hemochromatosis, symptomatic form of hemochromatosis type 1 |
| Doid Label | hemochromatosis type 1 |
| Doid Description | A hemochromatosis that has_material_basis_in homozygous or compound heterozygous mutation in the HFE gene on chromosome 6p22. |
| Disease Node Id | disease_node_17559 |
| Doid Id | DOID_0111029 |
| Disease Has Basis In | SO_0001537 |
| Label | Hemochromatosis Type 1 |
- Outgoing r'ship
SUBCLASS_OFto/from Hemochromatosis(ID:disease_node_3800) (Disease)