| dense deposit disease (aandoening) | | dense deposit disease | | DDD
| | Dense deposit disease | | Membranoproliferative glomerulonephritis type 2
MCGN (mesangiocapillary glomerulonephritis) type II
MPGNII - membranoproliferative glomerulonephritis type II
Mesangiocapillary glomerulonephritis type 2
| | A histological subtype of C3 glomerulopathy with characteristics of C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits. |
| | Id | 722760002 | | Status | Primitive |
| PALGA thesaurus simple reference set for pathology |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | N05.6 | | Term | Niet gespecificeerd nefritisch syndroom; Dense deposit disease |
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| SNOMED CT to Orphanet simple map | 93571 |
| SNOMED CT to ICD-10 extended map | | Target | N03.6 | | Rule | TRUE | | Advice | ALWAYS N03.6 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION | POSSIBLE REQUIREMENT FOR AN EXTERNAL CAUSE CODE | | Correlation | SNOMED CT source code to target map code correlation not specified |
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