Search Ontology:
Human Disease
hereditary pyropoikilocytosis
- Term ID
- DOID:0061026
- Synonyms
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- 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
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- MIM:266140
- ORDO:98867
- Ontology
- Human Disease ( DOID:0061026 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models