DVL3, dishevelled segment polarity protein 3, 1857

N. diseases: 167; N. variants: 6
Disease: Robinow Syndrome, Autosomal Dominant ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4551476
Disease: Robinow Syndrome, Autosomal Dominant
Robinow Syndrome, Autosomal Dominant 		0.320 GeneticVariation disease BEFREE Autosomal dominant Robinow syndrome associated with a novel DVL3 splice mutation. 29575616 2018
CUI: C4551476
Disease: Robinow Syndrome, Autosomal Dominant
Robinow Syndrome, Autosomal Dominant 		0.320 GeneticVariation disease BEFREE DVL3 Alleles Resulting in a -1 Frameshift of the Last Exon Mediate Autosomal-Dominant Robinow Syndrome. 26924530 2016
CUI: C4551476
Disease: Robinow Syndrome, Autosomal Dominant
Robinow Syndrome, Autosomal Dominant 		0.320 Biomarker disease CTD_human