WNT1, Wnt family member 1, 7471

N. diseases: 216; N. variants: 12
Disease: Osteoporosis, Senile ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0029459
Disease: Osteoporosis, Senile
Osteoporosis, Senile 		0.310 GeneticVariation disease BEFREE Our finding that homozygous and heterozygous variants in WNT1 predispose to low-bone-mass phenotypes might advance the development of more effective therapeutic strategies for congenital forms of bone fragility, as well as for common forms of age-related osteoporosis. 23499309 2013
CUI: C0029459
Disease: Osteoporosis, Senile
Osteoporosis, Senile 		0.310 Biomarker disease CTD_human