| hereditaire anetodermie (aandoening) | | hereditaire anetodermie | | erfelijke dermatitis atrophicans maculosa
erfelijke atrophia cutis maculosa
erfelijke maculaire atrofie
| | Hereditary anetoderma | | Hereditary macular atrophy
| | Familial anetoderma is an extremely rare genetic skin disease characterized by loss of elastin tissue leading to localized areas of flaccid skin and a family history of the disorder. |
| | DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | L90.8 | | Term | Overige gespecificeerde atrofische huidaandoeningen |
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| SNOMED CT to Orphanet simple map | 228277 |
| SNOMED CT to ICD-10 extended map | | Target | L90.8 | | Rule | TRUE | | Advice | ALWAYS L90.8 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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