enteropathy, familial, with villous edema and immunoglobulin G2 deficiency

Preferred Label : enteropathy, familial, with villous edema and immunoglobulin G2 deficiency;

Origin ID

C563949;

UMLS CUI

C1838238;

Currated CISMeF NLP mapping
- Enteropathy, familial, with villous edema and immunoglobulin g2 deficiency [OMIM Phenotype]
MeSH term(s) associated for indexing
- Primary Immunodeficiency Diseases [MeSH Descriptor]
- edema [MeSH Descriptor]
- immunologic deficiency syndromes [MeSH Descriptor]
- protein-losing enteropathies [MeSH Descriptor]
Record concept(s)
- enteropathy, familial, with villous edema and immunoglobulin G2 deficiency [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Enteropathy, familial, with villous edema and immunoglobulin g2 deficiency [OMIM Phenotype]