Nephrotic Syndrome Type 1

About the Disease
Nephrotic Syndrome, Type 1, also known as finnish congenital nephrosis, is related to nephrotic syndrome, type 2 and focal segmental glomerulosclerosis 1, and has symptoms including edema An important gene associated with Nephrotic Syndrome, Type 1 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 proteinuria and abnormal renal tubule morphology

Common Targets
CRB2 | NPHS1

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