Neurodevelopmental disorder with cerebellar ataxia and movement disorders

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Subtype of: Cerebellar ataxia · 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 ataxia and movement disorders
MONDO_0700092
KCND3 Unknown
23280837 23280838 25854634 26189493 28895081 28947073 31293010 33057194 34067185 39562497 40140957
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Neurodevelopmental disorder with cerebellar ataxia and movement disorders.
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Ectopic rhythm 1 shared geneKCND3 Related via 1 shared gene including KCND3. Hereditary ataxia 1 shared geneKCND3 Related via 1 shared gene including KCND3. Brugada syndrome 1 shared geneKCND3 Related via 1 shared gene including KCND3. Cardiac arrhythmia 1 shared geneKCND3 Related via 1 shared gene including KCND3. Spinocerebellar ataxia 1 shared geneKCND3 Related via 1 shared gene including KCND3.