Cystic fibrosis with pulmonary manifestations

Preferred Label : Cystic fibrosis with pulmonary manifestations;

Diag associé à un acte (%) : 64.4;

CMA : 2;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

E840;

UMLS CUI

C0348815;

Metaterm(s)
- pulmonology [CISMeF Metaterm]
Orphanet concepts
- Cystic fibrosis [ORDO Disease]
See also inter- (CISMeF)
- Classical cystic fibrosis [ICD-11 Subcategory]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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