Chromosome 19q13.11 deletion syndrome, proximal
MONDO:0014972Chromosome 19q13.11 deletion syndrome in which the proximal region was deleted.
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Disease
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Human disease
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Chromosomal disorder
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Developmental defect during embryogenesis
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Disease of genetic or genomic mechanism
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Multiple congenital anomalies/dysmorphic syndrome
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Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
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Autosomal anomaly
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Chromosome 19 disorder
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Chromosome 19q13.11 deletion syndrome
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