lymphangiectasis, intestinal

Preferred Label : lymphangiectasis, intestinal;

MeSH definition : Dilatation of the intestinal lymphatic system usually caused by an obstruction in the intestinal wall. It may be congenital or acquired and is characterized by DIARRHEA; HYPOPROTEINEMIA; peripheral and/or abdominal EDEMA; and PROTEIN-LOSING ENTEROPATHIES.;

MeSH synonym : intestinal lymphangiectases; lymphangiectases, intestinal; intestinal lymphangiectasis; lymphangiectasia, intestinal;

Details

Origin ID

D008201;

UMLS CUI

C0024215;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Exudative enteropathy (disorder) [SNOMED CT concept]
- Intestinal lymphangiectasia [ICD-11 Subcategory]
- Primary intestinal lymphangiectasia [ORDO Disease]
- Primary lymphangiectasis of intestine (disorder) [SNOMED CT concept]
- Protein-losing enteropathy [HPO term]
- Protein-losing enteropathy (disorder) [SNOMED CT concept]
- Waldmann disease [PASCAL descriptor]
- primary intestinal lymphangiectasia [SNOMED Notion]
- protein-losing enteropathy [SNOMED Notion]
Currated CISMeF NLP mapping
- Intestinal lymphangiectasia [HPO term]
- Intestinal lymphangiectasia [ORDO Disease]
- Intestinal lymphangiectasis (disorder) [SNOMED CT concept]
- Lymphangiectasia intestinal [MedDRA Preferred Term]
- Lymphangiectasia, intestinal [OMIM Phenotype]
- intestinal lymphangiectasia [Disease (Nov.)]
HPO term
- Intestinal lymphangiectasia [HPO term]
Manual NTBT mappings (CISMeF)
- Genetic intestinal disease [ORDO Disease]
- Rare intestinal disease [ORDO Disease]
- Secondary intestinal lymphangiectasia [ORDO Disease]
- Syndromic lymphedema [ORDO Disease]
Metaterm(s)
- hematology [CISMeF Metaterm]
ORDO relation(s)
- Intestinal lymphangiectasia [ORDO Disease]
Record concept(s)
- lymphangiectasis, intestinal [MeSH concept]
Related MeSH Supplementary Concept(s)
- aplasia cutis congenita intestinal lymphangiectasia [MeSH Supplementary Concept]
- hennekam lymphangiectasia lymphedema syndrome [MeSH Supplementary Concept]
- waldmann disease [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Intestinal lymphangiectasia [ORDO Disease]
- Intestinal lymphangiectasia [HPO term]
- Intestinal lymphangiectasis (disorder) [SNOMED CT concept]
- Lymphangiectasia intestinal [MedDRA Preferred Term]
- Lymphangiectasia, intestinal [OMIM Phenotype]
- intestinal lymphangiectasia [Disease (Nov.)]
Validated automatic mappings to BTNT
- Primary intestinal lymphangiectasia [ORDO Disease]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

recommendations
documents concerning education
documents for patients