Congenital syndrome characterized by a wide spectrum of characteristics including the absence of the THYMUS and PARATHYROID GLANDS resulting in T-cell immunodeficiency, HYPOCALCEMIA, defects in the outflow tract of the heart, and craniofacial anomalies.

Descriptor ID	D004062
MeSH Number(s)	C05.660.207.103.500 C14.240.400.021.500 C14.280.400.044.500 C15.604.451.249.500 C16.131.077.019.500 C16.131.240.400.021.500 C16.131.260.019.500 C16.131.482.249.500 C16.131.621.207.103.500 C16.320.180.019.500 C19.642.482.500.500
Concept/Terms	DiGeorge Syndrome DiGeorge Syndrome Syndrome, DiGeorge DiGeorge Sequence Familial Third and Fourth Pharyngeal Pouch Syndrome Autosomal Dominant Opitz G-Bbb Syndrome Autosomal Dominant Opitz G Bbb Syndrome Pharyngeal Pouch Syndrome Third and Fourth Pharyngeal Pouch Syndrome Thymic Aplasia Syndrome Catch22 DiGeorge Anomaly Hypoplasia of Thymus and Parathyroids Velocardiofacial Syndrome Velocardiofacial Syndrome Syndrome, Velocardiofacial Sedlackova Syndrome Syndrome, Sedlackova Shprintzen Syndrome Syndrome, Shprintzen 22q11.2DS VCF Syndrome Syndrome, VCF Velo-Cardio-Facial Syndrome Syndrome, Velo-Cardio-Facial Velo Cardio Facial Syndrome Deletion 22q11.2 Syndrome 22q11.2 Deletion Syndrome Deletion Syndrome, 22q11.2 Shprintzen VCF Syndrome Conotruncal Anomaly Face Syndrome Conotruncal Anomaly Face Syndrome Conotruncal Anomaly Face Syndrome (CTAF)

Below are MeSH descriptors whose meaning is more general than "DiGeorge Syndrome".

Below are MeSH descriptors whose meaning is related to "DiGeorge Syndrome".

Below are MeSH descriptors whose meaning is more specific than "DiGeorge Syndrome".