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Summary Literature (0)
DOID:0111631 - familial erythrocytosis 7


Disease Ontology Definition:A primary polycythemia characterized by high oxygen affinity hemoglobin and compensatory polycythemia that has_material_basis_in heterozygous mutation in either HBA2 or HBA1 on chromosome 16p13.3.

Synonyms: ECYT7, alpha-globin type erythrocytosis, alpha-globin type polycythemia

In OMIM:
OMIM:617981 - ERYTHROCYTOSIS, FAMILIAL, 7; ECYT7


Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : hba1, hba2

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): primary polycythemia (is_a)