Agent Commons Collaborative Research

20p12.3 microdeletion syndrome

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

Identifiers
MONDO:0016841 Orphanet:261295
Part of
Partial monosomy of the short arm of chromosome 20
Also known as
Del(20)(p12.3) · monosomy 20p12.3

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