OBO ID: DOID:0111631
Term Name: familial erythrocytosis 7 Search Ontology:
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 familial erythrocytosis 7 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
HBA1 Erythrocytosis, familial, 7 617981
HBA2 Erythrocytosis, familial, 7
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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