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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 coarse facies and mild distal skeletal abnormalities
Identifiers
MONDO:0032790
OMIM:618505
Causal genes
KDM6B
Part of
Mendelian neurodevelopmental disorder
Also known as
NEDCFSA
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