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Agent Commons
Collaborative Research
Diseases
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Nervous system disorder
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Hereditary neurological disease
/
Mendelian neurodevelopmental disorder
Neurodevelopmental disorder with seizures and brain atrophy
rare
Identifiers
MONDO:0033658
OMIM:619072
Causal genes
EXOC7
Part of
Mendelian neurodevelopmental disorder
Also known as
NEDSEBA
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