Symbol
| FSGS3
|
Location
| 6p12.3
|
Name
|
focal segmental glomerulosclerosis 3 |
Corresponding gene
|
CD2AP
|
Main clinical features
|
histopathologic finding in several renal disorders characterized by proteinuria and progressive decline in renal function
nephrotic syndrome with elevated urine microalbumin excretion without another cause (microalbumin more than 20 mg/g creatinine) |
Genetic determination
| autosomal recessive |
Related entries
| including hereditary/congenital nephrotic syndromes
|
Function/system disorder
| kidney and urinary tract |
Type
| disease
|