Koolen-de Vries syndrome due to a point mutation
MONDO:00182170 clinical trials for this condition and its sub-types.
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Disease
(647)
Hereditary disease
(176)
Human disease
(14)
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)
Disease by developmental or physiological process
(0)
Disease by etiologic mechanism
(0)
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