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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 impaired language, behavioral abnormalities, and dysmorphic facies
Identifiers
MONDO:0957588
OMIM:620494
Causal genes
UBAP2L
Part of
Mendelian neurodevelopmental disorder
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