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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 spasticity, thin corpus callosum, and decreased brain white matter
Identifiers
MONDO:0980947
OMIM:621460
Causal genes
RPS6KC1
Part of
Mendelian neurodevelopmental disorder
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