Disease Term Disease ID Gene Symbol Classification References Source
Properdin deficiency 2966 CFP Causal Pathogenic evidence from ClinVar - ClinVar
Properdin deficiency disease C0398762 CFP Causal Pathogenic evidence from ClinVar 6903190, 8871668 ClinVar
Properdin Deficiency, Type II C1839455 CFP Causal Pathogenic evidence from ClinVar - ClinVar
Properdin Deficiency, Type III C1839456 CFP Causal Pathogenic evidence from ClinVar - ClinVar