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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 speech impairment and dysmorphic facies
rare
Identifiers
MONDO:0033630
OMIM:619056
Causal genes
SETD1A
Part of
Mendelian neurodevelopmental disorder
Also known as
NEDSID
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