Other specified congenital malformations of intestine

Preferred Label : Other specified congenital malformations of intestine;

Inclusion CIM-10 : Congenital diverticulum, intestine; Transposition of colon; Dolichocolon; Congenital diverticulitis, colon; Megaloduodenum; Transposition of appendix; Microcolon; Congenital blind loop syndrome; Megaloappendix; Transposition of intestine;

Diag associé à un acte (%) : 99.6;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

Q438;

UMLS CUI

C0478034;

Automatic exact mappings (from CISMeF team)
- Congenital blind loop syndrome (disorder) [SNOMED CT concept]
- Dolichocolon [ICD-11 More detail]
- Dolichocolon [MedDRA Preferred Term]
- Dolichocolon [PASCAL descriptor]
- Dolichocolon (disorder) [SNOMED CT concept]
- Intestinal transposition [MedDRA Preferred Term]
- Megaloappendix [ICD-11 Subcategory]
- Megaloappendix (disorder) [SNOMED CT concept]
- Microcolon [NCIt concept]
- Microcolon [ICD-11 More detail]
- Microcolon [HPO term]
- Microcolon [MedDRA Preferred Term]
- Microcolon [OMIM Phenotype]
- Microcolon [PASCAL descriptor]
- Microcolon (disorder) [SNOMED CT concept]
- Transposition of appendix (disorder) [SNOMED CT concept]
- Transposition of colon (disorder) [SNOMED CT concept]
- Transposition of intestine (disorder) [SNOMED CT concept]
- megaduodenum [MeSH Supplementary Concept]
- microcolon [MeSH concept]
- microcolon [MeSH Supplementary Concept]
Excluded by
- Blind loop syndrome, not elsewhere classified [ICD-10 Sub-category]
- Diverticular disease of intestine [ICD-10 category]
Manual NTBT mappings (CISMeF)
- Congenital anal fissure (disorder) [SNOMED CT concept]
Orphanet concepts
- Congenital short bowel syndrome [ORDO Disease]
- Megacystis-microcolon-intestinal hypoperistalsis syndrome [ORDO Disease]
- Multiple intestinal atresia [ORDO Disease]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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