Alpha/beta t-cell lymphopenia with gamma/delta t-cell expansion, severe cytomegalovirus infection, and autoimmunity

Preferred Label : Alpha/beta t-cell lymphopenia with gamma/delta t-cell expansion, severe cytomegalovirus infection, and autoimmunity;

Type : Phenotype, molecular basis known;

Prefixed ID : #609889;

Details

Origin ID

609889;

UMLS CUI

C1835931;

Automatic exact mappings (from CISMeF team)
- Alpha-Beta T-Cell Lymphopenia with Gamma-Delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity [MeSH concept]
- Alpha-Beta T-Cell Lymphopenia with Gamma-Delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity [MeSH Supplementary Concept]
- Combined immunodeficiency due to partial RAG1 deficiency [ORDO Disease]
Genes related to phenotype
- Recombination-activating gene 1 [OMIM gene]
ORDO concept(s)
- Combined immunodeficiency due to partial RAG1 deficiency [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Alpha-Beta T-Cell Lymphopenia with Gamma-Delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity [MeSH Supplementary Concept]
- Alpha-Beta T-Cell Lymphopenia with Gamma-Delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity [MeSH concept]
- Combined immunodeficiency due to partial RAG1 deficiency [ORDO Disease]

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