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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 congenital cardiac defects and variable renal and ocular abnormalities
Identifiers
MONDO:0980965
OMIM:621474
Causal genes
KDM2B
Part of
Mendelian neurodevelopmental disorder
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