B3GALT6-congenital disorder of glycosylation

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
B3GALT6-congenital disorder of glycosylation
B3GALT6 Unknown — ClinGen
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with B3GALT6-congenital disorder of glycosylation.
5 View disease cluster →
Larsen syndrome 1 shared geneB3GALT6 Related via 1 shared gene including B3GALT6. Spondyloepiphyseal dysplasia 1 shared geneB3GALT6 Related via 1 shared gene including B3GALT6. Spondyloepimetaphyseal dysplasia 1 shared geneB3GALT6 Related via 1 shared gene including B3GALT6. Ehlers-danlos syndrome 1 shared geneB3GALT6 Related via 1 shared gene including B3GALT6. Bone fragility with contractures, arterial rupture, and deafness 1 shared geneB3GALT6 Related via 1 shared gene including B3GALT6.