| idiopathische non-lupus 'full-house' nefropathie (aandoening) | | idiopathische non-lupus 'full-house' nefropathie | | idiopathische non-lupus FHN
| | Idiopathic non-lupus full-house nephropathy | | Idiopathic non-lupus FHN (full-house nephropathy)
| | A rare idiopathic glomerular clinical syndrome with characteristics of diffuse renal lesions that are indistinguishable from the lesions observed in systemic lupus erythematosus (SLE) in the absence of circulating autoantibodies and other systemic features necessary to meet the classification criteria for SLE. Patients may present with nephrotic syndrome, abnormal urinary sediment, acute renal insufficiency, progressive glomerulonephritis and hypertension. Some patients have been reported to develop a progression to SLE over time. |
| | Id | 1260197005 | | Status | Primitive |
| SNOMED CT to Orphanet simple map | 567544 |
| SNOMED CT to ICD-10 extended map | | Target | N05.8 | | Rule | TRUE | | Advice | ALWAYS N05.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION | | Correlation | SNOMED CT source code to target map code correlation not specified |
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