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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 77
rare
Identifiers
MONDO:0031031
OMIM:619988
Causal genes
CEP104
Part of
Autosomal recessive non-syndromic intellectual disability
Also known as
MRT77
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