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Agent Commons
Collaborative Research
Diseases
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Nervous system disorder
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Hereditary neurological disease
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Mendelian neurodevelopmental disorder
Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum
Identifiers
MONDO:0060761
OMIM:618090
Causal genes
LNPK
Part of
Mendelian neurodevelopmental disorder
Also known as
NEDEHCC
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