Congenital cystic lung

Preferred Label : Congenital cystic lung;

Inclusion CIM-10 : Congenital cystic lung disease; Congenital honeycomb lung; Congenital polycystic lung disease;

ICD-10 exclusion note : cystic lung disease, acquired or unspecified (J98.4); cystic fibrosis (E84.0);

Diag associé à un acte (%) : 98.5;

CMA : 2;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

Q330;

UMLS CUI

C0158641;

Automatic exact mappings (from CISMeF team)
- Congenital cystic lung [MedDRA Preferred Term]
- Congenital cystic lung [ICD-9 code]
- Congenital cystic lung (disorder) [SNOMED CT concept]
- Congenital honeycomb lung (disorder) [SNOMED CT concept]
- Congenital pulmonary airway malformation [ORDO Disease]
- Congenital pulmonary airway malformation [HPO term]
- Congenital pulmonary airway malformations [ICD-11 Subcategory]
- Cystic lung, congenital [MedDRA LLT]
- congenital cystic lung [SNOMED Notion]
ICD-10 exclusion(s)
- Other disorders of lung [ICD-10 Sub-category]
Orphanet concepts
- Congenital pulmonary airway malformation [ORDO Disease]
- Congenital pulmonary airway malformation type 0 [ORDO Disease]
- Congenital pulmonary airway malformation type 1 [ORDO Disease]
- Congenital pulmonary airway malformation type 2 [ORDO Disease]
- Congenital pulmonary airway malformation type 3 [ORDO Disease]
- Congenital pulmonary airway malformation type 4 [ORDO Disease]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital cystic lung [MedDRA Preferred Term]
- Congenital cystic lung [ICD-9 code]
- Congenital cystic lung [MedDRA LLT]
- Congenital cystic lung (disorder) [SNOMED CT concept]
- Congenital pulmonary airway malformations [ICD-11 Subcategory]
- Cystic lung, congenital [MedDRA LLT]
- congenital cystic lung [SNOMED Notion]

Keyword's position in hierarchy(ies) :

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