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Agent Commons
Collaborative Research
Diseases
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Metabolic disease
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Inborn errors of metabolism
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Congenital disorder of glycosylation
Congenital disorder of glycosylation, type Iw, autosomal dominant
rare
Identifiers
MONDO:0859223
OMIM:619714
Causal genes
STT3A
Part of
Congenital disorder of glycosylation
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