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Summary Literature (0)
MIM:609820 - ERYTHROCYTOSIS, FAMILIAL, 3; ECYT3

Xenbase Genes: egln1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012353 - fin skeleton
MONDO:0016599 - obsolete autosomal dominant secondary polycythemia

Disease Ontology (DO):
DOID:0080338 - familial erythrocytosis 3