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Disease Ontology Browser
familial erythrocytosis 7 (DOID:0111631)
Alliance: disease page
Synonyms: alpha-globin type erythrocytosis; alpha-globin type polycythemia; ECYT7
Alt IDs: OMIM:617981
Definition: A primary polycythemia characterized by high oxygen affinity hemoglobin and compensatory polycythemia that has_material_basis_in heterozygous mutation in either the HBA2 or HBA1 gene on chromosome 16p13.3.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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04/16/2024
MGI 6.23 		The Jackson Laboratory