| mucopolysacharidose type 2 (aandoening) | | mucopolysacharidose type 2 | | sulfoïduronaatsulfatasedeficiëntie
MPS 2
syndroom van Hunter
| | syndroom van Hunter | | Erfelijke stofwisselingsziekte die alleen bij mannen voorkomt en skeletafwijkingen en beschadiging van organen veroorzaakt. | | Mucopolysaccharidosis, MPS-II | | Sulfoiduronidate sulfatase deficiency
Deficiency of iduronate-2-sulfatase
Hunter syndrome
Hunter disease
Iduronate 2-sulfatase deficiency
Sulfo-iduronate sulfatase deficiency
Mucopolysaccharidosis type II
Iduronate sulfatase deficiency
Hunter's syndrome
MPSII - Mucopolysaccharidosis type II
MPS 2 - Mucopolysaccharidosis 2
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| | Id | 70737009 | | 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 | E76.1 | | Term | Mucopolysaccharidose, type II |
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| SNOMED CT to Orphanet simple map | 580 |
| SNOMED CT to MedDRA simple map | 10056889 |
| SNOMED CT to ICD-10 extended map | | Target | E76.1 | | Rule | TRUE | | Advice | ALWAYS E76.1 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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