Source: UNIPROT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4920
Gene Symbol: ROR2
ROR2
CUI: C1849334
Disease: Robinow syndrome, autosomal recessive
Robinow syndrome, autosomal recessive 		1.000 GeneticVariation UNIPROT We detected several homozygous ROR2 mutations in our cohort of RRS patients that are located upstream from those previously found in BDB. 10932187

2000
Entrez Id: 4920
Gene Symbol: ROR2
ROR2
CUI: C1849334
Disease: Robinow syndrome, autosomal recessive
Robinow syndrome, autosomal recessive 		1.000 GeneticVariation UNIPROT Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2. 10932186

2000
Entrez Id: 4920
Gene Symbol: ROR2
ROR2
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.300 GeneticVariation UNIPROT