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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 dysmorphic facies and distal skeletal anomalies
rare
Identifiers
MONDO:0032855
OMIM:618659
Causal genes
ZMIZ1
Part of
Mendelian neurodevelopmental disorder
Also known as
NEDDFSA
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