| hereditaire myopathie met deficiëntie van succinaathydrogenase en aconitase (aandoening) | | hereditaire myopathie met deficiëntie van succinaathydrogenase en aconitase | | erfelijke myopathie met lactaatacidose
erfelijke myopathie met deficiëntie van succinaathydrogenase en aconitase
| | Myopathy with deficiency of iron-sulfur cluster assembly enzyme | | Myopathy with exercise intolerance, Swedish type
Hereditary myopathy with lactic acidosis
Myopathy with deficiency of iron-sulphur cluster assembly enzyme
Myoglobinuria due to abnormal glycolysis
Myopathy with deficiency of succinate dehydrogenase and aconitase
|
| | Id | 699268002 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | G71.3 | | Term | Mitochondriën-myopathie, niet elders geclassificeerd |
|
| SNOMED CT to Orphanet simple map | 43115 |
| SNOMED CT to ICD-10 extended map | | Target | G71.8 | | Rule | TRUE | | Advice | ALWAYS G71.8 | | Correlation | SNOMED CT source code to target map code correlation not specified |
|
|
