Chromosome 15q24 deletion syndrome
MONDO:001325615q24 microdeletion syndrome is a rare chromosomal anomaly characterized cytogenetically by a 1.7-6.1 Mb deletion in chromosome 15q24 and clinically by pre- and post-natal growth retardation, intellectual disability, distinct facial features, and genital, skeletal, and digital anomalies.
Also known as: 15q24 microdeletion syndrome, 15q24 recurrent microdeletion syndrome, Del(15)(q24), chromosome 15q24 deletion syndrome, monosomy 15q24, WITKOS, Witteveen-Kolk syndrome, chromosome 15Q24 Duplication syndrome
6 clinical trials for this condition and its sub-types.
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Disease
(618)
Hereditary disease
(172)
Human disease
(14)
Chromosomal disorder
(12)
Developmental defect during embryogenesis
(7)
Disease of genetic or genomic mechanism
(2)
Multiple congenital anomalies/dysmorphic syndrome
(1)
Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
(1)
Partial deletion of the long arm of chromosome 15
(1)
Disease by developmental or physiological process
(0)