6p22 microdeletion syndrome
MONDO:00166556p22 microdeletion syndrome is a newly described syndrome associated with a variable clinical phenotype including developmental delay, facial dysmorphism, short neck and diverse malformations.
Also known as: Del(6)(p22), monosomy 6p22
2 clinical trials for this condition and its sub-types.
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Disease
(618)
Human disease
(14)
Chromosomal disorder
(12)
Disease of genetic or genomic mechanism
(2)
Autosomal anomaly
(0)
Chromosome 6 disorder
(0)
Disease by etiologic mechanism
(0)
Partial deletion of chromosome 6
(0)
Partial deletion of the short arm of chromosome 6
(0)
Syndrome caused by partial chromosomal deletion
(0)