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DO Term : hereditary pyropoikilocytosis [DOID:0061026] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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.
  • synonyms:
  • OMIM:266140,
  • HPP,
  • 266140,
  • ORDO:98867
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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