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Paternal 14q32.2 microdeletion syndrome

MONDO:0016780

Also known as: paternal del(14)(q32.2), paternal monosomy 14q32.2

0 clinical trials for this condition and its sub-types, 0 tagged with Paternal 14q32.2 microdeletion syndrome itself.

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↑ Motor developmental delay due to 14q32.2 paternally expressed gene defect (0) ↑ Partial deletion of the long arm of chromosome 14 (0)

Including sub-types (0) Tagged with Paternal 14q32.2 microdeletion syndrome (0)

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