Congenital Nephrotic Syndrome

About the Disease
Familial Nephrotic Syndrome, also known as congenital nephrotic syndrome, is related to nephrotic syndrome, type 2 and nephrotic syndrome, type 21, and has symptoms including edema An important gene associated with Familial Nephrotic Syndrome is NPHS1 (NPHS1 Adhesion Molecule, Nephrin), and among its related pathways/superpathways are Cell junction organization and Primary focal segmental glomerulosclerosis (FSGS). Affiliated tissues include Kidney, placenta and brain, and related phenotypes are no effect and no effect

Common Targets
NPHS2 | LAMB2 | CD2AP | EHMT1 | ITGA3 | ARHGDIA | ACTN4 | PLCE1 | WT1 | BSN | TBC1D8B | TLN1 | COQ2 | MAGI2 | SGPL1 | NPHS1

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