Lowe-syndroom (aandoening) | | Lowe-syndroom | | syndroom van Lowe
| | syndroom van Lowe | | Lowe-syndroom
| | Erfelijke aandoening met als kenmerken een verstandelijke beperking, oogafwijkingen, onvoldoende spanning van de spieren en een ophoping van zuren in de nieren. | | Lowe syndrome | | Lowe-Terrey-MacLachlan syndrome Oculocerebrorenal syndrome Cerebro-oculorenal dystrophy Lowe disease Renal-oculocerebrodystrophy Oculocerebrorenal syndrome of Lowe Oculocerebrorenal dystrophy Phosphatidylinositol-4,5-bisphosphate-5-phosphatase deficiency Lowe-Bickel syndrome
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| Id | 79385002 | Status | Primitive |
PALGA thesaurus simple reference set for pathology |
DHD Diagnosis thesaurus reference set |
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | Target | E72.0 | Term | Stoornissen van aminozuurtransport |
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SNOMED CT to Orphanet simple map | 534 |
SNOMED CT to ICD-10 extended map | Target | E72.0 | Rule | TRUE | Advice | ALWAYS E72.0 | Correlation | SNOMED CT source code to target map code correlation not specified |
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