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DO Term : hemochromatosis type 2B [DOID:0111032] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A hemochromatosis type 2 that has_material_basis_in homozygous mutation in the HAMP gene on chromosome 19q13.

synonyms:
HFE2B,
613313,
OMIM:613313

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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