congenital absence of spleen

Preferred Label : congenital absence of spleen;

Origin ID

D4-C1020;

UMLS CUI

C0600031;

Automatic exact mappings (from CISMeF team)
- Bilateral right-sidedness sequence (disorder) [SNOMED CT concept]
- Congenital asplenia [ICD-11 Subcategory]
- Congenital malformations of spleen [ICD-10 Sub-category (who)]
Currated CISMeF NLP mapping
- Asplenia [HPO term]
- Asplenia [PASCAL descriptor]
- Asplenia [MedDRA Preferred Term]
- Congenital absence of spleen (disorder) [SNOMED CT concept]
- asplenia [Disease (Nov.)]
- asplenia [Radlex concept]
ICD-10 exact mapping(s)
- Congenital malformations of spleen [ICD-10 Sub-category (who)]
Metaterm(s)
- hematology [CISMeF Metaterm]
- pediatrics [CISMeF Metaterm]
Référence SNOMED
- congenital absence, nos [SNOMED Notion]
- spleen, nos [SNOMED Notion]
SNOMED CT concept
- Congenital absence of spleen (disorder) [SNOMED CT concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Agenesis of spleen (disorder) [SNOMED CT concept]
- Aplasia of spleen (disorder) [SNOMED CT concept]
- Asplenia [MedDRA Preferred Term]
- Asplenia [HPO term]
- Asplenia [PASCAL descriptor]
- Asplenia (disorder) [SNOMED CT concept]
- Congenital absence of spleen (disorder) [SNOMED CT concept]
- asplenia [Disease (Nov.)]
- asplenia [Radlex concept]
- congenital asplenia [Disease (Nov.)]
Validated automatic mappings to NTBT
- Aplasia of spleen (disorder) [SNOMED CT concept]