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Focal segmental glomerulosclerosis
? TBD
Kidney disease
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Subclasses
6
focal segmental glomerulosclerosis 5
focal segmental glomerulosclerosis that has material basis in an autosomal dominant mutation of INF2 on chromosome 14q32.33
focal segmental glomerulosclerosis 9
focal segmental glomerulosclerosis that has material basis in an autosomal recessive mutation of CRB2 on chromosome 9q33.3
focal segmental glomerulosclerosis 7
focal segmental glomerulosclerosis that has material basis in an autosomal dominant mutation of PAX2 on chromosome 10q24.31
focal segmental glomerulosclerosis 8
focal segmental glomerulosclerosis that has material basis in an autosomal dominant mutation of ANLN on chromosome 7p14.2
focal segmental glomerulosclerosis 2
focal segmental glomerulosclerosis that has material basis in a mutation of TRPC6 on chromosome 11q22.1
focal segmental glomerulosclerosis 6
focal segmental glomerulosclerosis that has material basis in an autosomal recessive mutation of MYO1E on chromosome 15q22.2
Subject of
1
Focal segmental glomerulosclerosis in children complicated by posterior reversible encephalopathy syndrome
scientific article published in January 2018
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Focal segmental glomerulosclerosis (FSGS) is a histopathologic finding of scarring (sclerosis) of glomeruli and damage to renal podocytes. This process damages the filtration function of the kidney, resulting in protein presence in the urine due to protein loss. FSGS is a leading cause of excess protein loss—nephrotic syndrome—in children and...

Instance of
Rare disease
class of disease
Subclass of
Glomerulosclerosis
Nephrotic syndrome
Disease
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