1p21.3 microdeletion syndrome
MONDO:00174051p21.3 microdeletion syndrome is an extremely rare chromosomal anomaly characterized by severe speech and language delay, intellectual deficiency, autism spectrum disorder.
Also known as: Del(1)p(21.3), monosomy 1p21.3
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 1 disorder
(0)
Disease by etiologic mechanism
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Partial deletion of chromosome 1
(0)
Partial deletion of the short arm of chromosome 1
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Syndrome caused by partial chromosomal deletion
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