3A73 Congenital dyserythropoietic anaemia

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

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)

synonyms

• Congenital dyserythropoietic anaemia
• congenital dyshaematopoietic anaemia
• CDA - [congenital dyserythropoietic anaemia]
• dyserythropoietic dyshaematopoietic congenital anaemia
• dyshaematopoietic anaemia
• dyserythropoietic anaemia
• Congenital dyserythropoietic anaemia type I
• CDA type 1 -[Congenital dyserythropoietic anaemia type 1]
• Congenital dyserythropoietic anaemia type II
• CDA type 2 - [Congenital dyserythropoietic anaemia type 2]
• Congenital dyserythropoietic anaemia type III
• CDA type 3 - [Congenital dyserythropoietic anaemia type 3]
• Dyserythropoietic anaemia with thrombocytopenia
• X-linked dyserythropoietic anaemia and thrombocytopenia

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