PRCP, prolylcarboxypeptidase, 5547

N. diseases: 68; N. variants: 7
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0398625
Disease: Protein C Deficiency
Protein C Deficiency
0.010 GeneticVariation disease BEFREE These results, obtained in a small series of patients, suggest that both the ProC Global assay and the PCP Test would be suitable, using well-defined cut-off levels, to identify all the carriers of the Factor V Leiden mutation and all the patients with a protein C deficiency or with combined defects of the protein C pathway. 10806561 2000