3A73
category
Congenital dyserythropoietic anaemia
Definition
Congenital dyserythropoietic anaemias (CDA) result from diverse erythropoietic disorders; they lead to the defective production of red blood cells (RBC) and often mild haemolysis that attests to a qualitative defect of these RBC released into the circulation. Three forms of CDA have been characterised: types I, II and III. The shared symptoms include anaemia of variable severity, intermittent jaundice, splenomegaly and hepatomegaly.
Exclusions
- Blackfan-Diamond syndrome
(3A60.1) - Di Guglielmo disease
(2A60.35)
Also indexed as
CDA - [congenital dyserythropoietic anaemia]CDA type 1 -[Congenital dyserythropoietic anaemia type 1]CDA type 2 - [Congenital dyserythropoietic anaemia type 2]CDA type 3 - [Congenital dyserythropoietic anaemia type 3]Congenital dyserythropoietic anaemiaCongenital dyserythropoietic anaemia type ICongenital dyserythropoietic anaemia type IICongenital dyserythropoietic anaemia type IIIDyserythropoietic anaemia with thrombocytopeniaX-linked dyserythropoietic anaemia and thrombocytopeniacongenital dyshaematopoietic anaemiadyserythropoietic anaemiadyserythropoietic dyshaematopoietic congenital anaemiadyshaematopoietic anaemia