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DO Term : familial erythrocytosis 7 [DOID:0111631] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  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.
  • synonyms:
  • 617981,
  • alpha-globin type erythrocytosis,
  • alpha-globin type polycythemia,
  • ECYT7,
  • OMIM:617981
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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