Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Familial Hypophosphatemic Rickets
CUI: C3536983
Disease: Familial Hypophosphatemic Rickets
0.010 GeneticVariation BEFREE Vitamin D-resistant rickets and type 1 diabetes in a child with compound heterozygous mutations of the vitamin D receptor (L263R and R391S): dissociated responses of the CYP-24 and rel-B promoters to 1,25-dihydroxyvitamin D3. 16753019 2006