WNT5A, Wnt family member 5A, 7474

N. diseases: 375; N. variants: 11
Disease: ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4551475
Disease: ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1 		0.600 GeneticVariation disease UNIPROT WNT5A mutations in patients with autosomal dominant Robinow syndrome. 19918918 2010
CUI: C4551475
Disease: ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1 		0.600 Biomarker disease GENOMICS_ENGLAND WNT5A mutations in patients with autosomal dominant Robinow syndrome. 19918918 2010
CUI: C4551475
Disease: ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1 		0.600 Biomarker disease GENOMICS_ENGLAND
CUI: C4551475
Disease: ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1 		0.600 CausalMutation disease CLINVAR
CUI: C4551475
Disease: ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1 		0.600 GeneticVariation disease CLINVAR