congenital disorder of glycosylation, type Iw, autosomal dominant

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
congenital disorder of glycosylation, type Iw, autosomal dominant
STT3A Causal
34653363
ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with congenital disorder of glycosylation, type Iw, autosomal dominant.
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