Disease: Van der Woude syndrome 2 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1847604
Disease: Van der Woude syndrome 2
Van der Woude syndrome 2 		0.700 GeneticVariation disease UNIPROT Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm development. 24360809 2014
CUI: C1847604
Disease: Van der Woude syndrome 2
Van der Woude syndrome 2 		0.700 CausalMutation disease CLINVAR
CUI: C1847604
Disease: Van der Woude syndrome 2
Van der Woude syndrome 2 		0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C1847604
Disease: Van der Woude syndrome 2
Van der Woude syndrome 2 		0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C1847604
Disease: Van der Woude syndrome 2
Van der Woude syndrome 2 		0.700 Biomarker disease CTD_human