| dystrofia bullosa hereditaria typus maculatus (aandoening) | | dystrofia bullosa hereditaria typus maculatus | | erythrokeratodermia variabilis
syndroom van Mendes da Costa
| | Erythrokeratodermia variabilis | | Congenital poikiloderma
Mendes da Costa syndrome
|
| | Id | 70041004 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | Q82.8 | | Term | Overige gespecificeerde congenitale misvormingen van huid |
|
| SNOMED CT to Orphanet simple map | 317 |
| SNOMED CT to ICD-10 extended map | | Target | Q82.8 | | Rule | TRUE | | Advice | ALWAYS Q82.8 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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