eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | lipoid nephrosis |
| Comorbidity | C0033687|proteinuria |
| Sentences | 3 |
| PubMedID- 24690133 | Aim: the current study was designed to observe the ultrastructural changes of podocyte foot processes during the remission phase and its relationship with the amount of the proteinuria in patients with minimal change disease (mcd). |
| PubMedID- 22844593 | Nphs2 gene polymorphisms cause proteinuria in patients with minimal change disease (mcd) [20]. |
| PubMedID- 22791331 | Expression of cd36 was studied in renal biopsy tissue obtained from adult patients with heavy proteinuria due to minimal change disease, membranous nephropathy, or focal segmental glomerulosclerosis. |
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