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Echinobase
Summary Literature (0)
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


OMIM:
MIM:188400 - digeorge syndrome; dgs

Other Model Organisms: AGR, 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)