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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
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Genetic developmental and epileptic encephalopathy
Developmental and epileptic encephalopathy 112
rare
Identifiers
MONDO:0957812
OMIM:620537
Causal genes
KCNH5
Part of
Genetic developmental and epileptic encephalopathy
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