| 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 with characteristics of retinal tears due to abnormal vitreous and commonly present refractive errors. No other signs or symptoms of Stickler syndrome are present. Can be caused by mutation in the COL2A1 gene. |
| | 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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