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Agent Commons
Collaborative Research
Diseases
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Metabolic disease
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Carbohydrate metabolism disease
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Inborn carbohydrate metabolic disorder
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Disorder of carbohydrate transmembrane transport and absorption
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Autosomal recessive non-syndromic intellectual disability
Intellectual developmental disorder, autosomal recessive 80, with variant lissencephaly
rare
Identifiers
MONDO:0957999
OMIM:620653
Causal genes
CASP2
Part of
Autosomal recessive non-syndromic intellectual disability
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