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DO Term : hemochromatosis type 2A [DOID:0111027] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A hemochromatosis type 2 that has_material_basis_in homozygous or compound heterozygous mutation in the HJV gene on chromosome 1q21.

synonyms:
602390,
HFE2A,
OMIM:602390

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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