| congenitaal defect in glycosylering type 1A (aandoening) | | congenitaal defect in glycosylering type 1A | | congenital disorder of glycosylation type 1a
|  | Dit betekent dat de suikers in je lichaam niet goed samen kunnen werken met je eiwitten en vetten. Hierdoor kun je problemen krijgen met je gezondheid. Je bent hiermee geboren. | | Congenital disorder of glycosylation type Ia | | Carbohydrate deficient glycoprotein syndrome type Ia
Congenital disorder of glycosylation type 1a
PMM2-CDG (congenital disorder of glycosylation)
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| | Id | 459063003 | | Status | Primitive |
| SNOMED CT to Orphanet simple map |
| DHD Diagnosis thesaurus reference set |
| SNOMED CT to ICD-10 extended map | | Target | E77.8 | | Rule | TRUE | | Advice | ALWAYS E77.8 | 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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| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | E77.8 | | Term | Overige gespecificeerde stoornissen van glycoproteïnemetabolisme |
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