Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter

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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 ataxic gait, absent speech, and decreased cortical white matter
MONDO_0060624
RAB11B Causal
19344873 29106825 39502218
Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter.
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Intellectual disability 1 shared geneRAB11B Related via 1 shared gene including RAB11B. Neurodevelopmental disorder 1 shared geneRAB11B Related via 1 shared gene including RAB11B. Metabolic syndrome 1 shared geneRAB11B Related via 1 shared gene including RAB11B. Diabetes mellitus type 2 1 shared geneRAB11B Related via 1 shared gene including RAB11B.