| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | A T cell deficiency disease that is the result of a large deletion of chromosome 22 which includes the DGS gene needed for development of the thymus and related glands with subsequent lack of T-cell production. (Human Disease Ontology, DOID_11198) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:D004062 |
| Similar Terms | |
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5 genes/proteins associated with the disease DiGeorge Syndrome from the curated CTD Gene-Disease Associations dataset.
