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Summary Literature (0)
MIM:133100 - ERYTHROCYTOSIS, FAMILIAL, 1; ECYT1

Xenbase Genes: epor, sh2b3, jak2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007572 - primary familial polycythemia due to EPO receptor mutation

Disease Ontology (DO):
DOID:0060652 - familial erythrocytosis 1