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
6 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsBroader categories
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)
Autosomal anomaly
(0)
Chromosome 17 disorder
(0)