| multifocale patroondystrofie van retinaal pigmentepitheel lijkend op fundus flavimaculatus (aandoening) | | multifocale patroondystrofie van retinaal pigmentepitheel lijkend op fundus flavimaculatus | | ziekte van Stargardt simulerende multifocale patroondystrofie van retinaal pigmentepitheel
| | Multifocal pattern dystrophy of retinal pigment epithelium simulating fundus flavimaculatus | | Multifocal pattern dystrophy simulating fundus flavimaculatus
Multifocal pattern dystrophy simulating Stargardt disease
| | A rare, patterned dystrophy of the retinal pigment epithelium characterized by multiple yellowish irregular flecks scattered or interconnected around the macula, simulating what is observed in Stargardt disease, and usually asymptomatic until adulthood when patients present with a slowly progressive loss of vision that often only becomes apparent in old age. |
| | Id | 723408004 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | H35.5 | | Term | Hereditaire retinadystrofie |
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| SNOMED CT to Orphanet simple map | 99003 |
| SNOMED CT to ICD-10 extended map | | Target | H35.5 | | Rule | TRUE | | Advice | ALWAYS H35.5 | 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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