10p13-p14 deletion syndrome
MONDO:09759050 clinical trials 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)
Multiple congenital anomalies/dysmorphic syndrome
(1)
Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
(1)
Autosomal anomaly
(0)
Chromosome 10 disorder
(0)
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