disease has location syndrome caused by partial chromosomal deletion congenital T-cell immunodeficiency digestive system disease DiGeorge syndrome 22q deletion syndrome(s) 22q11.2 Deletion syndrome A congenital anomaly characterized by immunodeficiency, abnormal facies, congenital heart disease, hypocalcemia, and increased susceptibility to infections. Pathologic characteristics include conotruncal abnormalities and absence or hypoplasia of thymus and parathyroid glands. DiGeorge syndrome is associated with abnormalities of chromosome 22. Also known as DiGeorge anomaly. Catch22 DGS DGS1 DOID:11198 Di-George syndrome DiGeorge anomaly DiGeorge sequence DiGeorge syndrome DiGeorge syndrome chromosome region DiGeorge syndrome type 1 DiGeorge's syndrome GTR:AN1145678 ICD10:D82.1 ICD9:279.11 MESH:D004062 MONDO:0008564 NCIT:C2989 OMIM:188400 SCTID:77128003 Shprintzen syndrome Sphrintzen Takao VCF syndrome UMLS:CN734570 VCF chromosome 22Q11.2 deletion syndrome hypoplasia of thymus and parathyroids pharyngeal pouch syndrome third and fourth pharyngeal pouch syndrome velo-cardio-facial syndrome velocardiofacial syndrome 22q11.2 deletion syndrome neurocristopathy pharyngeal pouch