WormBase Tree Display for DO_term: DOID:0111028
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DOID:0111028 | Name | hemochromatosis type 4 | |||
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Status | Valid | ||||
Definition | A hemochromatosis that has_material_basis_in heterozygous mutation in the SLC40A1 gene on chromosome 2q32. | ||||
Synonym | Exact | HFE4 | |||
autosomal dominant hereditary hemochromatosis | |||||
ferroportin disease | |||||
hemochromatosis due to defect in ferroportin | |||||
Parent | Is_a | DOID:2352 | |||
DB_info | Database | OMIM | disease | 606069 | |
Attribute_of | Gene_by_orthology | WBGene00019977 | |||
WBGene00021354 |