Disease: Confusion ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0009676
Disease: Confusion
Confusion 		0.110 AlteredExpression phenotype BEFREE In two male sons, this mutation caused a severe (< 3%) deficiency of ADAMTS-13 activity and antigen level, associated with periodic thrombocytopenia, haemolytic anaemia and mild mental confusion. 26272487 2016
CUI: C0009676
Disease: Confusion
Confusion 		0.110 Biomarker phenotype HPO