Xp22.13p22.2 duplication syndrome
MONDO:0017284Also known as: Duplication Xp22, dup(X)(p22), dup(X)(p22.13p22.2)
5 clinical trials for this condition and its sub-types.
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Disease
(680)
Human disease
(14)
Chromosomal disorder
(12)
Developmental defect during embryogenesis
(8)
Gonosome anomaly
(6)
Disease of genetic or genomic mechanism
(2)
Multiple congenital anomalies/dysmorphic syndrome
(1)
Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
(1)
Chromosome X disorder
(0)
Disease by developmental or physiological process
(0)