Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction

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Subtype of: Neurodevelopmental disorder
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
neurodevelopmental disorder with cerebellar atrophy and motor dysfunction
MONDO_0859152
GEMIN5 Causal
33963192
ClinGen, Open Targets
All1 Causal1 Unknown0
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