Koolen-de Vries syndrome due to 17q21.31 microdeletion syndrome
MONDO:0018216Also known as: 17q21.31 recurrent microdeletion syndrome, Del(17)(q21.31), monosomy 17q21.31
1 clinical trial for this condition and its sub-types.
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Disease
(680)
Hereditary disease
(176)
Human disease
(14)
Chromosomal disorder
(12)
Developmental defect during embryogenesis
(8)
Disease of genetic or genomic mechanism
(2)
Koolen-de Vries syndrome
(1)
Multiple congenital anomalies/dysmorphic syndrome
(1)
Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
(1)
Autosomal anomaly
(0)