| autosomaal dominante bèta-2-microglobuline-amyloïdose (aandoening) | | autosomaal dominante bèta-2-microglobuline-amyloïdose | | Aβ2M-amyloïdose
| | Autosomal dominant beta2-microglobulinic amyloidosis | | Variant ABeta2M amyloidosis
| | A rare form of amyloidosis characterized by accumulation and extensive visceral deposition of an amyloidogenic variant of beta 2 microglobulin leading to progressive gastrointestinal dysfunction, Sjögren syndrome and autonomic neuropathy. |
| | Id | 722292000 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | E85.1 | | Term | Neuropathische heredofamiliale amyloïdose |
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| SNOMED CT to Orphanet simple map | 314652 |
| SNOMED CT to ICD-10 extended map | | Target | E85.1 | | Rule | TRUE | | Advice | ALWAYS E85.1 | 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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