Congenital absence and malformations of spleen

Preferred Label : Congenital absence and malformations of spleen;

ICD-10 exclusion note : isomerism of atrial appendages (with asplenia or polysplenia) (Q20.6);

Diag associé à un acte (%) : 88.8;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

Q890;

UMLS CUI

C2910349;

Automatic exact mappings (from CISMeF team)
- Congenital anomaly of spleen (disorder) [SNOMED CT concept]
- Congenital malposition of spleen (disorder) [SNOMED CT concept]
Excluded by
- Hypersplenism [ICD-10 Sub-category]
- Hyposplenism [ICD-10 Sub-category]
ICD-10 exclusion(s)
- Isomerism of atrial appendages [ICD-10 Sub-category]
Orphanet concepts
- Familial isolated congenital asplenia [ORDO Disease]
- Isolated splenogonadal fusion [ORDO Disease]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
Validated automatic mappings to BTNT
- Structural developmental anomalies of spleen [ICD-11 Category]

Keyword's position in hierarchy(ies) :

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