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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 ataxia, hypotonia, and microcephaly
rare
Identifiers
MONDO:0032816
OMIM:618569
Causal genes
SVBP
Part of
Mendelian neurodevelopmental disorder
Also known as
NEDAHM
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