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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 hearing loss and spasticity
rare
Identifiers
MONDO:0859206
OMIM:619616
Orphanet:659975
Causal genes
AFG2B
Part of
Mendelian neurodevelopmental disorder
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