|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A combined T cell and B cell immunodeficiency that is caused by a defect in several genes encoding for B and T lymphocytes resulting in individuals with non-functional immune systems. (Human Disease Ontology, DOID_627)|
|Downloads & Tools|
4 genes/proteins associated with the disease Severe Combined Immunodeficiency from the curated CTD Gene-Disease Associations dataset.