MMRN1, multimerin 1, 22915

N. diseases: 272; N. variants: 3
Disease: Hereditary Factor V Deficiency ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0015499
Disease: Hereditary Factor V Deficiency
Hereditary Factor V Deficiency 		0.010 Biomarker disease BEFREE Recent studies identified multimerin as a specific coagulation factor V binding protein, complexed with platelet, but not plasma, factor V. These findings led us to investigate individuals with inherited factor V deficiencies for possible multimerin abnormalities. 8652809 1996