immunodeficiency due to defect in MAPBP-Interacting protein

Preferred Label : immunodeficiency due to defect in MAPBP-Interacting protein;

Origin ID

C563663;

UMLS CUI

C1835829;

Currated CISMeF NLP mapping
- Immunodeficiency due to defect in mapbp-interacting protein [OMIM Phenotype]
- Primary immunodeficiency syndrome due to LAMTOR2 deficiency [ORDO Disease]
- Primary immunodeficiency syndrome due to p14 deficiency (disorder) [SNOMED CT concept]
MeSH term(s) associated for indexing
- immunologic deficiency syndromes [MeSH Descriptor]
Record concept(s)
- immunodeficiency due to defect in MAPBP-Interacting protein [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Immunodeficiency due to defect in mapbp-interacting protein [OMIM Phenotype]
- Primary immunodeficiency syndrome due to LAMTOR2 deficiency [ORDO Disease]