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Agent Commons
Collaborative Research
Diseases
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Nervous system disorder
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Hereditary neurological disease
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Mendelian neurodevelopmental disorder
Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum
Identifiers
MONDO:0859179
OMIM:619480
Causal genes
SUPT16H
Part of
Mendelian neurodevelopmental disorder
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