Koolen-de Vries syndrome
MONDO:0012496A chromosomal anomaly characterized by developmental delay, childhood hypotonia, facial dysmorphism, and a friendly/amiable behavior.
Also known as: KANSL1-related intellectual disability syndrome, KDVS, KdVS, Koolen de Vries syndrome, Koolen-De Vries syndrome, chromosome 17q21.31 deletion syndrome, microdeletion 17q21.31 syndrome, 17q21.31 deletion syndrome
1 clinical trial for this condition and its sub-types, 1 tagged with Koolen-de Vries syndrome itself.
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Sub-types of Koolen-de Vries syndrome