3p25.3 microdeletion syndrome
MONDO:0018564A rare chromosomal anomaly characterized by intellectual disability, epilepsy or EEG abnormalities, poor speech, ataxia, and stereotypic hand movements.
Also known as: Del(3)p(25.3), intellectual disability-epilepsy-stereotypic hand movement syndrome, monosomy 3p25.3
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 3 disorder
(0)
Disease by etiologic mechanism
(0)
Partial deletion of chromosome 3
(0)
Partial deletion of the short arm of chromosome 3
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Syndrome caused by partial chromosomal deletion
(0)
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