Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum

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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 epilepsy and hypoplasia of the corpus callosum
MONDO_0060761
LNPK Causal
30032983 37794925 35599435
Open Targets —
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum.
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Abnormality of the cerebellum 1 shared geneLNPK Related via 1 shared gene including LNPK. Hypoplasia of the corpus callosum 1 shared geneLNPK Related via 1 shared gene including LNPK. Generalized hypotonia 1 shared geneLNPK Related via 1 shared gene including LNPK. Exostoses 1 shared geneLNPK Related via 1 shared gene including LNPK. Carpal tunnel syndrome 1 shared geneLNPK Related via 1 shared gene including LNPK.