Mhc class II deficiency 5

Preferred Label : Mhc class II deficiency 5;

Symbol : MHC2D5;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Bare lymphocyte syndrome, type II, complementation group e;

Prefixed ID : #620818;

Details

Origin ID

620818;

UMLS CUI

C1859538;

Genes related to phenotype
- Regulatory factor X, 5 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- bare lymphocyte syndrome, type II, complementation group E [MeSH concept]

Keyword's position in hierarchy(ies) :

You can consult :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients