anemia, dyserythropoietic, congenital

Preferred Label : anemia, dyserythropoietic, congenital;

UMLS semantic type : T047 - Disease or Syndrome;

Détails

Origin ID

M0001122;

UMLS CUI

C0002876;

Currated CISMeF NLP mapping
- Anemia, congenital dyserythropoietic [OMIM phenotypic series]
- Congenital Dyserythropoietic Anemia [NCIt concept]
- Congenital dyserythropoietic anaemia [ICD-11 Category]
- Congenital dyserythropoietic anaemia [ICD-10 Sub-category (who)]
- Congenital dyserythropoietic anemia [ICD-10 Sub-category]
- Congenital dyserythropoietic anemia [PASCAL descriptor]
- Congenital dyserythropoietic anemia [MedDRA LLT]
- Congenital dyserythropoietic anemia [ORDO Disease]
- Congenital dyserythropoietic anemia (disorder) [SNOMED CT concept]
- congenital dyserythropoietic anemia [Disease (Nov.)]
- congenital dyserythropoietic anemia [DO Concept]
- congenital dyserythropoietic anemia, nos [SNOMED Notion]
False automatic mappings
- Congenital hypoplastic anemia [HPO term]
MeSH narrower concept(s)
- anemia, dyserythropoietic, congenital, type I [MeSH concept]
- anemia, dyserythropoietic, congenital, type II [MeSH concept]
- anemia, dyserythropoietic, congenital, type III [MeSH concept]
Related record
- anemia, dyserythropoietic, congenital [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital Dyserythropoietic Anemia [NCIt concept]
- Congenital dyserythropoietic anaemia [ICD-10 Sub-category (who)]
- Congenital dyserythropoietic anaemia [MedDRA Preferred Term]
- Congenital dyserythropoietic anemia [ORDO Disease]
- Congenital dyserythropoietic anemia [ICD-10 Sub-category]
- Congenital dyserythropoietic anemia [MedDRA LLT]
- Congenital dyserythropoietic anemia (disorder) [SNOMED CT concept]
- congenital dyserythropoietic anemia [DO Concept]
- congenital dyserythropoietic anemia [Disease (Nov.)]
- congenital dyserythropoietic anemia, nos [SNOMED Notion]

Position du mot-clé dans l'(les) arborescence(s) :

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