先天性红细胞生成异常性贫血 / Congenital dyserythropoietic anaemia

Congenital dyserythropoietic anemias (CDA) result from diverse erythropoietic disorders; they lead to the defective production of red blood cells (RBC) and often mild hemolysis that attests to a qualitative defect of these RBC released into the circulation. Three forms of CDA have been characterized: types I, II and III. The shared symptoms include anemia of variable severity, intermittent jaundice, splenomegaly and hepatomegaly.

http://purl.bmicc.cn/ontology/ICD11CN/3A73

Congenital dyserythropoietic anemias (CDA) result from diverse erythropoietic disorders; they lead to the defective production of red blood cells (RBC) and often mild hemolysis that attests to a qualitative defect of these RBC released into the circulation. Three forms of CDA have been characterized: types I, II and III. The shared symptoms include anemia of variable severity, intermittent jaundice, splenomegaly and hepatomegaly.

Blackfan-Diamond syndrome (3A60.1)

Di Guglielmo disease (2A60.35)

http://id.who.int/icd/release/11/2019-04/mms/899830967

先天性红细胞生成异常性贫血 / Congenital dyserythropoietic anaemia

http://purl.bmicc.cn/ontology/ICD10CN/D64.4

3A73

ICD11CN:A73

先天性红细胞生成异常性贫血 / Congenital dyserythropoietic anaemia

http://purl.bmicc.cn/ontology/ICD11CN/L1-3A0