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DO Term : hemochromatosis type 1 [DOID:0111029] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A hemochromatosis that has_material_basis_in homozygous or compound heterozygous mutation in the HFE gene on chromosome 6p22.

synonyms:
ORDO:465508,
ICD10CM:E83.1,
OMIM:235200,
symptomatic form of hemochromatosis type 1,
235200,
symptomatic form of HFE-related hereditary hemochromatosis,
HFE1,
GARD:10417,
symptomatic form of classic hemochromatosis

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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