Jacobsen syndrome

MONDO:0007838

A multiple congenital anomaly/intellectual disability contiguous gene syndrome caused by partial deletion of the long arm of chromosome 11.

Also known as: 11q terminal deletion disorder, Del(11)(q23.3), Del(11)(qter), Jacobsen syndrome, Jacobsen syndrome, Isolated cases, distal deletion 11q, distal monosomy 11q, monosomy 11qter

39 clinical trials for this condition and its sub-types.

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