20p12.3 microdeletion syndrome

MONDO:0016841

20p12.3 microdeletion syndrome is a recently described syndrome characterized by Wolff-Parkinson-White syndrome, variable developmental delay and facial dysmorphism.

Also known as: Del(20)(p12.3), monosomy 20p12.3

0 clinical trials for this condition and its sub-types, 0 tagged with 20p12.3 microdeletion syndrome itself.

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Part of

↑ Partial monosomy of the short arm of chromosome 20 (0)

Including sub-types (0) Tagged with 20p12.3 microdeletion syndrome (0)

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