Mhc class II deficiency 3

Preferred Label : Mhc class II deficiency 3;

Symbol : MHC2D3;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Bare lymphocyte syndrome, type II, Complementation group C;

Prefixed ID : #620816;

Détails

Origin ID

620816;

UMLS CUI

C1859536;

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 C [MeSH concept]

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