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16p13.11 microduplication syndrome
MONDO:001683716p13.11 microduplication syndrome is a recently described syndrome associated with variable clinical features including behavioral abnormalities, developmental delay, congenital heart defects and skeletal anomalies.
Also known as: 16p13.11 recurrent microduplication (neurocognitive disorder susceptibility locus), dup(16)(p13.11), trisomy 16p13.11
2 clinical trials for this condition and its sub-types.
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Disease
(618)
Human disease
(14)
Chromosomal disorder
(12)
Disease of genetic or genomic mechanism
(2)
Autosomal anomaly
(0)
Chromosome 16 disorder
(0)
Disease by etiologic mechanism
(0)
Partial duplication of chromosome 16
(0)
Partial duplication of the short arm of chromosome 16
(0)
Syndrome caused by partial chromosomal duplication
(0)