20p12.3 microdeletion syndrome
MONDO:001684120p12.3 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.
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Disease
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Human disease
(14)
Chromosomal disorder
(12)
Disease of genetic or genomic mechanism
(2)
Autosomal anomaly
(0)
Chromosome 20 disorder
(0)
Disease by etiologic mechanism
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Partial deletion of chromosome 20
(0)
Partial monosomy of the short arm of chromosome 20
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Syndrome caused by partial chromosomal deletion
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