Maternal 14q32.2 microdeletion syndrome
MONDO:0016781Also known as: maternal del(14)(q32.2), maternal monosomy 14q32.2
0 clinical trials for this condition and its sub-types.
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Disease
(717)
Human disease
(15)
Developmental defect during embryogenesis
(8)
Multiple congenital anomalies/dysmorphic syndrome
(1)
Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
(1)
Disease by developmental or physiological process
(0)
Disorder of development or morphogenesis
(0)
Multiple congenital anomalies due to 14q32.2 imprinting defect
(0)
Multiple congenital anomalies due to 14q32.2 maternally expressed gene defect
(0)
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