bare lymphocyte syndrome, type II, complementation group A

Preferred Label : bare lymphocyte syndrome, type II, complementation group A;

CISMeF synonym : bare lymphocyte syndrome, type II, complementation group B; bare lymphocyte syndrome, type II, complementation group C; bare lymphocyte syndrome, type II, complementation group D; bare lymphocyte syndrome, type II, complementation group E;

Détails

Origin ID

C565910;

UMLS CUI

C1859534;

Automatic exact mappings (from CISMeF team)
- Mhc class II deficiency 1 [OMIM Phenotype]
MeSH term(s) associated for indexing
- severe combined immunodeficiency [MeSH Descriptor]
Record concept(s)
- bare lymphocyte syndrome, type II, complementation group A [MeSH concept]
- bare lymphocyte syndrome, type II, complementation group B [MeSH concept]
- bare lymphocyte syndrome, type II, complementation group C [MeSH concept]
- bare lymphocyte syndrome, type II, complementation group D [MeSH concept]
- bare lymphocyte syndrome, type II, complementation group E [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Mhc class II deficiency 1 [OMIM Phenotype]

Position du mot-clé dans l'(les) arborescence(s) :

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