| syndroom van microcornea, posterieure megalolenticonus, persisterende foetale vasculatuur en coloboom (aandoening) | | syndroom van microcornea, posterieure megalolenticonus, persisterende foetale vasculatuur en coloboom | | syndroom van microcornea, megalolenticonus posterior, persistente foetale vasculatuur en coloboom
| | Microcornea, posterior megalolenticonus, persistent fetal vasculature, coloboma syndrome | | MPPC (microcornea, posterior megalolenticonus, persistent fetal vasculature, coloboma) syndrome
| | A rare developmental defect of the eye with characteristics of bilateral microcornea, posterior megalolenticonus, persistent fetal vasculature (extending from the posterior pole of the lens to the optic disc) and posterior chorioretinal coloboma. |
| | Id | 773690008 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | Q15.8 | | Term | Overige gespecificeerde congenitale misvormingen van oog |
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| SNOMED CT to Orphanet simple map | 231736 |
| SNOMED CT to ICD-10 extended map | | Target | Q15.8 | | Rule | TRUE | | Advice | ALWAYS Q15.8 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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