FZD2, frizzled class receptor 2, 2535

N. diseases: 139; N. variants: 6
Disease: Robinow Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0265205
Disease: Robinow Syndrome
Robinow Syndrome 		0.500 GermlineCausalMutation disease ORPHANET WNT Signaling Perturbations Underlie the Genetic Heterogeneity of Robinow Syndrome. 29276006 2018
CUI: C0265205
Disease: Robinow Syndrome
Robinow Syndrome 		0.500 Biomarker disease GENOMICS_ENGLAND A mutation in FRIZZLED2 impairs Wnt signaling and causes autosomal dominant omodysplasia. 25759469 2015