Mhc class II deficiency 2

Preferred Label : Mhc class II deficiency 2;

Symbol : MHC2D2;

Type : Phenotype, molecular basis known;

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

Prefixed ID : #620815;

Details

Origin ID

620815;

UMLS CUI

C1859535;

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

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