Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language

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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 thin corpus callosum, hypotonia, and absent language
MONDO_0976263
EEF1D Causal
30787422 28097321 36576126 38083972
Open Targets
All1 Causal1 Unknown0
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