Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0026267
Disease: Mitral Valve Prolapse Syndrome
Mitral Valve Prolapse Syndrome
0.400 Biomarker disease CTD_human New recessive truncating mutation in LTBP3 in a family with oligodontia, short stature, and mitral valve prolapse. 25899461 2015
CUI: C0026267
Disease: Mitral Valve Prolapse Syndrome
Mitral Valve Prolapse Syndrome
0.400 Biomarker disease HPO