| autosomaal dominante regmatogene netvliesloslating (aandoening) | | autosomaal dominante regmatogene netvliesloslating | | autosomaal dominante regmatogene ablatio retinae
| | Autosomal dominant rhegmatogenous retinal detachment | | A rare, hereditary, non-syndromic form of vitreoretinopathy characterized by retinal tears due to abnormal vitreous, and commonly present refractive errors. No other signs or symptoms of Stickler syndrome is present. |
| | Id | 773727009 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | H33.0 | | Term | Netvliesloslating met netvliesscheur |
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| SNOMED CT to Orphanet simple map | 209867 |
| SNOMED CT to ICD-10 extended map | | Target | H33.0 | | Rule | TRUE | | Advice | ALWAYS H33.0 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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