Summary
Properdin Deficiency, X-Linked, also known as properdin deficiency,is related to properdin deficiency and mccune-albright syndrome, somatic, mosaic,and has symptoms including abnormality of metabolism/homeostasis and dysfunctional alternative complement pathway. An important gene associated with Properdin Deficiency, X-Linked is CFP (Complement Factor Properdin), and among its related pathways is Immune response Lectin induced complement pathway
All SNPs
Genes | SNP | Risk Alleles |
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