Search Ontology:
Human Disease

familial erythrocytosis 7

Term ID
DOID:0111631
Synonyms
  • alpha-globin type erythrocytosis
  • alpha-globin type polycythemia
  • ECYT7
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. (2)
References
Ontology
Human Disease   ( DOID:0111631 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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