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Disease Ontology Browser
familial erythrocytosis 3 (DOID:0080338)
Alliance: disease page
Alt IDs: OMIM:609820
Definition: A primary polycythemia that has_material_basis_in heterozygous mutation in the EGLN1 gene on chromosome 1q42.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
03/19/2019
MGI 6.13
The Jackson Laboratory