CFP, complement factor properdin, 5199

N. diseases: 108; N. variants: 7
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0025294
Disease: Meningococcal meningitis
Meningococcal meningitis
0.300 Biomarker disease CTD_human Molecular characterisation of 10 Dutch properdin type I deficient families: mutation analysis and X-inactivation studies. 10909851 2000
CUI: C0025294
Disease: Meningococcal meningitis
Meningococcal meningitis
0.300 Biomarker disease CTD_human Sequence-based analysis of properdin deficiency: identification of point mutations in two phenotypic forms of an X-linked immunodeficiency. 8530058 1995