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ENC3 Glomerulopathy (DDD)
Alias:
C3 Glomerulonephritis
Non-Immunoglobulin-Mediated Membranoproliferative Glomerulonephritis
C3g
Non-Ig-Mediated Membranoproliferative Glomerulonephritis
Membranoproliferative Glomerulonephritis, Type Ii
Membranoproliferative Glomerulonephritis Type Ii
Glomerulonephritis with Dominant C3
Non-Immunoglobulin-Mediated Mpgn
Dense Deposit Disease
Non-Ig-Mediated Mpgn
Ddd/mpgnii
Ddd
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C3 Glomerulopathy, also known as c3 glomerulonephritis, is related to complement factor i deficiency and dense deposit disease. An important gene associated with C3 Glomerulopathy is CFHR5 (Complement Factor H Related 5), and among its related pathways/superpathways are Innate Immune System and Diseases of hemostasis. The drugs Pharmaceutical Solutions and Complement C3 have been mentioned in the context of this disorder. Affiliated tissues include kidney and retina, and related phenotypes are hematuria and hypertension
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