| idiopathische membraneuze glomerulonefritis (aandoening) | | idiopathische membraneuze glomerulonefritis | | Idiopathic membranous glomerulonephritis | | Idiopathic membranous nephropathy
| | A rare glomerular disease, histologically characterized by thickening of the capillary wall, with immune deposits predominantly containing IgG4 and C3 on the sub-epithelial side, and typically manifesting with nephrotic syndrome. |
| | DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | N03.2 | | Term | Chronisch nefritisch syndroom met diffuse membraneuze glomerulonefritis |
|
| SNOMED CT to Orphanet simple map | 97560 |
| SNOMED CT to ICD-10 extended map | | Target | N04.2 | | Rule | TRUE | | Advice | ALWAYS N04.2 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION | | Correlation | SNOMED CT source code to target map code correlation not specified |
|
|
