Hypophosphatemic rickets, autosomal recessive, 2

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Subtype of: Hypophosphatemic rickets
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Hypophosphatemic rickets, autosomal recessive, 2
MONDO_0013219
ENPP1 Causal
20137772 20137773 12881724 22209248 15605415 11159191 15940697 19206175 25741938 20016754
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. Arterial calcification, generalized, of infancy, 1 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.