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DO Term : familial erythrocytosis 3 [DOID:0080338] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A primary polycythemia that has_material_basis_in heterozygous mutation in the EGLN1 gene on chromosome 1q42.

synonyms:
OMIM:609820,
609820,
ECYT3

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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