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Echinobase
Summary Literature (0)
DOID:0080338 - familial erythrocytosis 3

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

Synonyms: ECYT3,

Echinobase Genes :


OMIM:
MIM:609820 - erythrocytosis, familial, 3; ecyt3

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), primary polycythemia (is_a)