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DOID:11198 - DiGeorge syndrome
Disease Ontology Definition: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.
Synonyms: DiGeorge sequence (disorder), DiGeorge's syndrome, Pharyngeal pouch syndrome,
Echinobase Genes : tbx1
MIM:188400 - digeorge syndrome; dgs |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
chromosomal deletion syndrome (is_a),
syndrome (is_a)