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ENFamilial Nephrotic Syndrome
Alias:
Congenital Nephrotic Syndrome
Nephrosis, Congenital
Finnish Congenital Nephrotic Syndrome
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Familial Nephrotic Syndrome, also known as congenital nephrotic syndrome, is related to nephrotic syndrome, type 2 and nephrotic syndrome, type 4, 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 and placenta, and related phenotypes are renal/urinary system and nervous system
Related ID：
MESH：C535761
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MALACARDS
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