Chromosome 17p13.3 duplication syndrome
MONDO:001318217p13.3 microduplication syndrome is characterized by variable psychomotor delay and dysmorphic features.
Also known as: 17p13.3 duplication syndrome, 17p13.3 microduplication syndrome, dup(17)(p13.3), trisomy 17p13.3, chromosome 17p13.3, centromeric, DUPLICATION syndrome
0 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)
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)
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