Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Immune system disorder · Heart disorder · Congenital nervous system disorder · Multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome · Chromosome 22q deletion
22q11.2 deletion syndrome
22q11.2 deletion syndrome (DS) is a chromosomal anomaly which causes a congenital malformation disorder whose common features include cardiac defects, palatal anomalies, facial dysmorphism, developmental delay and immune deficiency.
-
DiGeorge syndrome 11 trials
-
Velocardiofacial syndrome 4 trials