Congenital disorder of glycosylation, type Iw, autosomal dominant

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Subtype of: Congenital disorder of glycosylation
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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
MONDO_0014270
STT3A Causal
23842455 28424003 30701557 34653363
ClinGen, Open Targets
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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Congenital disorder of glycosylation 1 shared geneSTT3A Related via 1 shared gene including STT3A. Attention deficit hyperactivity disorder 1 shared geneSTT3A Related via 1 shared gene including STT3A. Bipolar disorder 1 shared geneSTT3A Related via 1 shared gene including STT3A. Autism 1 shared geneSTT3A Related via 1 shared gene including STT3A. Major depressive disorder 1 shared geneSTT3A Related via 1 shared gene including STT3A.