Arterial calcification, generalized, of infancy, 1

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Subtype of: Arterial calcification, generalized, of infancy
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
arterial calcification, generalized, of infancy, 1
MONDO_0008817
ENPP1 Causal
11159191 12881724 15605415 15940697 19206175 19521093 19813208 20016754 20137772 20137773 22209248 23430823 25741938 27467858 31742715
ClinGen, Open Targets
All1 Causal1 Unknown0
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Cole disease 1 shared geneENPP1 Related via 1 shared gene including ENPP1. Coronary medial sclerosis of infancy 1 shared geneENPP1 Related via 1 shared gene including ENPP1. Hypopigmentation-punctate palmoplantar keratoderma syndrome 1 shared geneENPP1 Related via 1 shared gene including ENPP1. Generalised arterial calcification of infancy and hypophosphatemic rickets 1 shared geneENPP1 Related via 1 shared gene including ENPP1. Hypophosphatemic rickets, autosomal recessive, 2 1 shared geneENPP1 Related via 1 shared gene including ENPP1.