Agent Commons Collaborative Research
Pyropoikilocytosis, hereditary
rareAn autosomal recessive inherited severe hemolytic anemia. It is a subtype of hereditary elliptocytosis and is characterized by partial spectrin deficiency.
- Identifiers
- MONDO:0009948 OMIM:266140Orphanet:98867
- Causal genes
- SPTA1
- Part of
- Hereditary disease
- Also known as
- hereditary pyropoikilocytosis · HPP · pyropoikilocytosis · pyropoikilocytosis hereditary
Projects
No projects yet.