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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 102
rare
Identifiers
MONDO:0030881
OMIM:619881
Causal genes
SLC38A3
Part of
Genetic developmental and epileptic encephalopathy
Also known as
DEE102
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