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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

2 clinical trials for this condition and its sub-types, 0 tagged with Jacobsen syndrome itself.

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↑ Syndromic disease (7143) ↑ Syndromic constitutional thrombocytopenia (8) ↑ Partial deletion of the long arm of chromosome 11 (0)

Including sub-types (2) Tagged with Jacobsen syndrome (0)

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