Congenital dyserythropoietic anemia

Preferred Label : Congenital dyserythropoietic anemia;

Inclusion CIM-10 : Dyshematopoietic anemia (congenital);

ICD-10 exclusion note : Di Guglielmo's disease (C94.0); Blackfan-Diamond syndrome (D61.01);

Diag associé à un acte (%) : 59.3;

Autres : 2;

CMA : 2;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

D644;

UMLS CUI

C0002876;

Currated CISMeF NLP mapping
- Anemia, congenital dyserythropoietic [OMIM phenotypic series]
- Congenital Dyserythropoietic Anemia [NCIt concept]
- Congenital dyserythropoietic anaemia [ICD-10 Sub-category (who)]
- Congenital dyserythropoietic anaemia [ICD-11 Category]
- Congenital dyserythropoietic anemia [ORDO Disease]
- Congenital dyserythropoietic anemia [PASCAL descriptor]
- Congenital dyserythropoietic anemia [MedDRA LLT]
- 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 [Disease (Nov.)]
- congenital dyserythropoietic anemia [DO Concept]
- congenital dyserythropoietic anemia, nos [SNOMED Notion]
DO Cross reference
- congenital dyserythropoietic anemia [DO Concept]
ICD-10 exclusion(s)
- Acute erythroid leukemia [ICD-10 Sub-category]
- Constitutional aplastic anemia [ICD-10 Sub-category]
Manual NTBT mappings (CISMeF)
- Pancreatic insufficiency-anemia-hyperostosis syndrome [ORDO Disease]
- Thrombocytopenia with congenital dyserythropoietic anemia [ORDO Disease]
Orphanet concepts
- Congenital dyserythropoietic anemia [ORDO Disease]
- Congenital dyserythropoietic anemia type I [ORDO Disease]
- Congenital dyserythropoietic anemia type II [ORDO Disease]
- Congenital dyserythropoietic anemia type III [ORDO Disease]
- Congenital dyserythropoietic anemia type IV [ORDO Disease]
- Constitutional dyserythropoietic anemia [ORDO Disease]
- X-linked dyserythropoietic anemia with abnormal platelets and neutropenia [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital Dyserythropoietic Anemia [NCIt concept]
- Congenital dyserythropoietic anaemia [MedDRA Preferred Term]
- Congenital dyserythropoietic anemia [ORDO Disease]
- Congenital dyserythropoietic anemia [MedDRA LLT]
- Congenital dyserythropoietic anemia (disorder) [SNOMED CT concept]
- anemia, dyserythropoietic, congenital [MeSH Descriptor]
- anemia, dyserythropoietic, congenital [MeSH concept]
- congenital dyserythropoietic anemia [DO Concept]
- congenital dyserythropoietic anemia [Disease (Nov.)]
- congenital dyserythropoietic anemia, nos [SNOMED Notion]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients