Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly

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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 ataxia, hypotonia, and microcephaly
EFO_0010560
SVBP Causal
30607023 31363758 26350204
Open Targets —
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly.
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Non-specific syndromic intellectual disability 1 shared geneSVBP Related via 1 shared gene including SVBP. Intellectual developmental disorder 1 shared geneSVBP Related via 1 shared gene including SVBP. Neurodevelopmental disorder 1 shared geneSVBP Related via 1 shared gene including SVBP.