Lymphangiectasia, intestinal

Preferred Label : Lymphangiectasia, intestinal;

Type : Phenotype or locus, molecular basis unknown;

Inheritance : Autosomal dominant;

Prefixed ID : %152800;

Details

Origin ID

152800;

UMLS CUI

C0024215;

Automatic exact mappings (from CISMeF team)
- Intestinal lymphangiectasia [ICD-11 Subcategory]
- Primary intestinal lymphangiectasia [ORDO Disease]
- 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]
- intestinal lymphangiectasia [Disease (Nov.)]
- lymphangiectasis, intestinal [MeSH Descriptor]
- lymphangiectasis, intestinal [MeSH concept]
HPO term(s)
- Abnormal hair morphology [HPO term]
- Autosomal dominant inheritance [HPO term]
- Decreased circulating IgG level [HPO term]
- Edema [HPO term]
- Intestinal lymphangiectasia [HPO term]
- Lymphopenia [HPO term]
- Malabsorption [HPO term]
- Neonatal hypoproteinemia [HPO term]
- Pedal edema [HPO term]
- Prominent floating ribs [HPO term]
- Stillbirth [HPO term]
- Stillbirth [HPO term]
ORDO concept(s)
- Primary intestinal lymphangiectasia [ORDO Disease]
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]
- intestinal lymphangiectasia [Disease (Nov.)]
- lymphangiectasis, intestinal [MeSH Descriptor]
- lymphangiectasis, intestinal [MeSH concept]

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