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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 intention tremor, pyramidal signs, dyspraxia, and ocular anomalies
Identifiers
MONDO:0859274
OMIM:619995
Causal genes
SMG9
Part of
Mendelian neurodevelopmental disorder
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