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Metadata
ID	DOID:0080338
Name	familial erythrocytosis 3
Definition	A primary polycythemia that has_material_basis_in heterozygous mutation in the EGLN1 gene on chromosome 1q42. https://www.ncbi.nlm.nih.gov/pubmed/16407130
Xrefs	MIM:609820
Synonyms	ECYT3 [EXACT]
Parent Relationships	is_a primary polycythemia is_a autosomal dominant disease
Subclass Logical Relationships	has material basis in some autosomal dominant inheritance