| mucopolysacharidose type 2 (aandoening) | | mucopolysacharidose type 2 | | sulfoïduronaatsulfatasedeficiëntie
MPS 2
syndroom van Hunter
|  | Dit betekent dat je lichaam bepaalde stoffen niet goed kan verwerken. Dit komt door een fout in je DNA. Er blijven afvalstoffen achter in je lichaam. Hierdoor kun je problemen krijgen in verschillende delen van je lichaam. | | 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 |
| SNOMED CT to Orphanet simple map |
| SNOMED CT to MedDRA simple map |
| 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 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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