16p13.11 microduplication syndrome

MONDO:0016837

16p13.11 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

0 clinical trials for this condition and its sub-types, 0 tagged with 16p13.11 microduplication syndrome itself.

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Part of

↑ Partial duplication of the short arm of chromosome 16 (0)

Including sub-types (0) Tagged with 16p13.11 microduplication syndrome (0)

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