| Preferred Name |
Congenital Combined Immunodeficiency |
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C27871 |
| code |
C27871 |
| Concept_In_Subset | |
| Contributing_Source |
CTRP |
| DEFINITION |
A broad classification of inherited disorders presenting at birth that affect both the cell-mediated and humoral aspects of the immune response. Circulating numbers of B lymphocytes, T lymphocytes and NK cells are variable but where present do not function properly. Susceptibility to infection is the primary concern. |
| Display_Name |
Congenital Combined Immunodeficiency |
| label |
Congenital Combined Immunodeficiency |
| Legacy_Concept_Name |
Congenital_Combined_Immunodeficiency |
| Preferred_Name |
Congenital Combined Immunodeficiency |
| prefixIRI |
C27871 |
| prefLabel |
Congenital Combined Immunodeficiency |
| Semantic_Type |
Disease or Syndrome |
| UMLS_CUI |
C0494261 |
| subClassOf |
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| There are currently no mappings for this class. | |||