Gene: FZD2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2535
Gene Symbol: FZD2
FZD2 		0.500 GermlineCausalMutation disease ORPHANET WNT Signaling Perturbations Underlie the Genetic Heterogeneity of Robinow Syndrome. 29276006 2018
Entrez Id: 2535
Gene Symbol: FZD2
FZD2 		0.500 Biomarker disease GENOMICS_ENGLAND A mutation in FRIZZLED2 impairs Wnt signaling and causes autosomal dominant omodysplasia. 25759469 2015