Chromosome 17q21.31 duplication syndrome
MONDO:0013298The newly described 17q21.31 microduplication syndrome is associated with a broad clinical spectrum, of which behavioral disorders and poor social interaction seem to be the most consistent.
Also known as: 17q21.31 microduplication syndrome, chromosome 17q21.31 duplication syndrome, dup(17)(q21.31), trisomy 17q21.31
0 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsBroader categories
Disease
(680)
Human disease
(14)
Chromosomal disorder
(12)
Developmental defect during embryogenesis
(8)
Disease of genetic or genomic mechanism
(2)
Multiple congenital anomalies/dysmorphic syndrome
(1)
Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
(1)
Autosomal anomaly
(0)
Chromosome 17 disorder
(0)
Disease by developmental or physiological process
(0)
We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.