Congenital dyserythropoietic anaemia

ICD-11 code : 3A73;

Preferred Label : Congenital dyserythropoietic anaemia;

ICD-11 definition : 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.;

ICD-11 synonym : congenital dyshaematopoietic anaemia; CDA - [congenital dyserythropoietic anaemia];

ICD-11 acronym : CDA;

ICD-11 inclusion : dyserythropoietic anaemia; dyshaematopoietic anaemia; dyserythropoietic dyshaematopoietic congenital anaemia;

Details

Origin ID

899830967;

Automatic exact mappings (from CISMeF team)
- CDA Gene [NCIt concept]
- Congenital anomaly of blood, blood-forming organs and immune system [ICPC-3 diagnosis]
- Corneal dystrophy, avellino type [OMIM Phenotype]
- Cytidine deaminase [OMIM gene]
- dermatitis, atopic [MeSH Descriptor]
Currated CISMeF NLP mapping
- Congenital Dyserythropoietic Anemia [NCIt concept]
- Congenital dyserythropoietic anaemia [MedDRA Preferred Term]
- Congenital dyserythropoietic anemia [PASCAL descriptor]
- Congenital dyserythropoietic anemia [ORDO Disease]
- Congenital dyserythropoietic anemia [ICD-10 Sub-category]
- Congenital dyserythropoietic anemia (disorder) [SNOMED CT concept]
- Congenital hypoplastic anemia [HPO term]
- anemia, dyserythropoietic, congenital [MeSH concept]
- anemia, dyserythropoietic, congenital [MeSH Descriptor]
- congenital dyserythropoietic anemia [DO Concept]
- congenital dyserythropoietic anemia, nos [SNOMED Notion]
False automatic mappings
- Cladribine [NCIt concept]
ICD-10 Mapping
- Congenital dyserythropoietic anemia [ICD-10 Sub-category]

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