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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 microcephaly, hypotonia, nystagmus, and seizures
Identifiers
MONDO:0859250
OMIM:619876
Causal genes
CPSF3
Part of
Mendelian neurodevelopmental disorder
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