Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7474
Gene Symbol: WNT5A
WNT5A
0.600 GeneticVariation disease UNIPROT WNT5A mutations in patients with autosomal dominant Robinow syndrome. 19918918 2010
Entrez Id: 7474
Gene Symbol: WNT5A
WNT5A
0.600 Biomarker disease GENOMICS_ENGLAND WNT5A mutations in patients with autosomal dominant Robinow syndrome. 19918918 2010
Entrez Id: 7474
Gene Symbol: WNT5A
WNT5A
0.600 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 7474
Gene Symbol: WNT5A
WNT5A
0.600 CausalMutation disease CLINVAR
Entrez Id: 7474
Gene Symbol: WNT5A
WNT5A
0.600 GeneticVariation disease CLINVAR
Entrez Id: 4920
Gene Symbol: ROR2
ROR2
0.300 Biomarker disease GENOMICS_ENGLAND A novel single-base deletion in ROR2 causes atypical brachydactyly type B1 with cutaneous syndactyly in a large Chinese family. 19461659 2009
Entrez Id: 1857
Gene Symbol: DVL3
DVL3
0.100 CausalMutation disease CLINVAR DVL3 Alleles Resulting in a -1 Frameshift of the Last Exon Mediate Autosomal-Dominant Robinow Syndrome. 26924530 2016