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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
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CACNA1C-related disorder
Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures
rare
Identifiers
MONDO:0859286
OMIM:620029
Part of
CACNA1C-related disorder
Mendelian neurodevelopmental disorder
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