Mhc class II deficiency 4

Preferred Label : Mhc class II deficiency 4;

Symbol : MHC2D4;

Type : Phenotype, molecular basis known;

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

Prefixed ID : #620817;

Détails

Origin ID

620817;

UMLS CUI

C1859537;

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

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