CFP, complement factor properdin, 5199

N. diseases: 108; N. variants: 7
Disease: Properdin Deficiency, Type III ×
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C1839456
Disease: Properdin Deficiency, Type III
Properdin Deficiency, Type III 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases Disease or Syndrome 1 1 0.100 None 0 1