Hypersplenism - CISMeF

Preferred Label : Hypersplenism;

ICD-10 exclusion note : splenitis, splenomegaly in late syphilis (A52.79); primary splenic neutropenia (D73.81); splenomegaly congenital (Q89.0); splenitis, splenomegaly in tuberculosis (A18.85); neutropenic splenomegaly (D73.81); splenomegaly NOS (R16.1);

Diag associé à un acte (%) : 90.8;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

D731;

UMLS CUI

C0020532;

Currated CISMeF NLP mapping
- Hypersplenism [NCIt concept]
- Hypersplenism [MedDRA Preferred Term]
- Hypersplenism [HPO term]
- Hypersplenism [HRDO Sign]
- Hypersplenism [ICD-9 code]
- Hypersplenism [PASCAL descriptor]
- Hypersplenism [ICD-11 Subcategory]
- Hypersplenism [ICD-10 Sub-category (who)]
- Hypersplenism (disorder) [SNOMED CT concept]
- hypersplenism [MeSH concept]
- hypersplenism [MeSH Descriptor]
- hypersplenism [Disease (Nov.)]
- hypersplenism [DO Concept]
- hypersplenism, nos [SNOMED Notion]
DO Cross reference
- hypersplenism [DO Concept]
ICD-10 exclusion(s)
- Congenital absence and malformations of spleen [ICD-10 Sub-category]
- Splenomegaly, not elsewhere classified [ICD-10 Sub-category]
Metaterm(s)
- hematology [CISMeF Metaterm]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hypersplenism [MedDRA Preferred Term]
- Hypersplenism [ICD-9 code]
- Hypersplenism [HPO term]
- Hypersplenism [NCIt concept]
- Hypersplenism [HRDO Sign]
- Hypersplenism [PASCAL descriptor]
- Hypersplenism [ICD-11 Subcategory]
- Hypersplenism (disorder) [SNOMED CT concept]
- hypersplenism [MeSH Descriptor]
- hypersplenism [MeSH concept]
- hypersplenism [DO Concept]
- hypersplenism [Disease (Nov.)]
- hypersplenism, nos [SNOMED Notion]

Keyword's position in hierarchy(ies) :

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