Disease: Syndactyly ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0039075
Disease: Syndactyly
Syndactyly 		0.110 GeneticVariation disease BEFREE To the best of our knowledge, the deletion represents the second ROR2 mutation associated with a BDB1-syndactyly phenotype. 19461659 2009
CUI: C0039075
Disease: Syndactyly
Syndactyly 		0.110 Biomarker disease HPO