CFH, complement factor H, 3075

N. diseases: 393; N. variants: 150
Disease: Familial Thrombotic Thrombocytopenic Purpura ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1956258
Disease: Familial Thrombotic Thrombocytopenic Purpura
Familial Thrombotic Thrombocytopenic Purpura 		0.010 GeneticVariation disease BEFREE Complement factor H mutation in familial thrombotic thrombocytopenic purpura with ADAMTS13 deficiency and renal involvement. 15800115 2005