congenital dyserythropoietic anemia
MONDO:0019403Mondo
Findings
No curated finding names congenital dyserythropoietic anemia yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Congenital dyserythropoietic anemia (CDA) is a heterogenous group of hematological disorders of late erythropoiesis and red cell abnormalities that lead to anemia. Five types of CDA are defined: CDA I, CDA II, CDA III, CDA IV and thrombocytopenia with CDA.
Definition from the Mondo Disease Ontology (MONDO:0019403), read 2026-09-29. CC BY 4.0.
Genes
2 genes
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
Where it sits
- A kind of
- Narrower terms (9)
- Anemia, congenital dyserythropoietic, type IIIb, autosomal recessive
- anemia, congenital dyserythropoietic, type IVb
- congenital dyserythropoietic anemia type 1
- congenital dyserythropoietic anemia type 2
- congenital dyserythropoietic anemia type 3
- congenital dyserythropoietic anemia type 4
- pancreatic insufficiency-anemia-hyperostosis syndrome
- thrombocytopenia with congenital dyserythropoietic anemia
- X-linked dyserythropoetic anemia with abnormal platelets and neutropenia
Other names
4 names
Resolves to: congenital dyserythropoietic anemia
- Also called
- anemia, congenital dyserythropoieticCDAcongenital dyshaematopoietic anaemiacongenital dyshaematopoietic anemia