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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
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Bryant-Li-Bhoj neurodevelopmental syndrome
Bryant-Li-Bhoj neurodevelopmental syndrome 2
rare
Identifiers
MONDO:0030607
OMIM:619721
Causal genes
H3-3B
Part of
Bryant-Li-Bhoj neurodevelopmental syndrome
Also known as
BRYLIB2
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