Search Ontology:
Human Disease

hereditary pyropoikilocytosis

Term ID
DOID:0061026
Synonyms
  • HPP
Definition
A hemolytic anemia characterized by microspherocytosis, poikilocytosis, and an unusual thermal sensitivity of red cells that has_material_basis_in mutation in the alpha-spectrin or the beta-spectrin gene. https://pubmed.ncbi.nlm.nih.gov/1191563/
References
Ontology
Human Disease   ( DOID:0061026 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models