Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0220697
Disease: POLYDACTYLY, POSTAXIAL
POLYDACTYLY, POSTAXIAL
0.110 GeneticVariation disease BEFREE C5orf42 mutations result in a purely neurological Joubert phenotype, in one case associated with postaxial polydactyly. 25920555 2016
CUI: C0220697
Disease: POLYDACTYLY, POSTAXIAL
POLYDACTYLY, POSTAXIAL
0.110 Biomarker disease HPO