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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
Poirier-Bienvenu neurodevelopmental syndrome
rare
Identifiers
MONDO:0032889
OMIM:618732
Orphanet:689397
Causal genes
CSNK2B
Part of
Mendelian neurodevelopmental disorder
Also known as
POBINDS
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