Disease: Congenital vascular anomaly ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1961121
Disease: Congenital vascular anomaly
Congenital vascular anomaly 		0.010 GeneticVariation group BEFREE The majority of vascular anomalies had associated mutations that commonly affected tyrosine kinase receptor signaling through the RAS or PIK3CA pathways. 29697621 2018