Other congenital malformations of esophagus

Preferred Label : Other congenital malformations of esophagus;

Inclusion CIM-10 : Congenital displacement of esophagus; Congenital absence of esophagus; Congenital duplication of esophagus;

Diag associé à un acte (%) : 99.1;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

Q398;

UMLS CUI

C0478028;

Automatic exact mappings (from CISMeF team)
- Congenital absence of esophagus (disorder) [SNOMED CT concept]
- Congenital displacement of esophagus (disorder) [SNOMED CT concept]
- Congenital duplication of esophagus (disorder) [SNOMED CT concept]
- Esophageal Duplication [NCIt concept]
Orphanet concepts
- Duplication of the esophagus [ORDO Disease]
- Esophageal duplication cyst [ORDO Disease]
- Tubular duplication of the esophagus [ORDO Disease]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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