| mucopolysacharidose type 4 (aandoening) | | mucopolysacharidose type 4 | | syndroom van Morquio
| | syndroom van Morquio | | Erfelijke stofwisselingsziekte gekenmerkt door skeletafwijkingen, oogproblemen en een grof gezicht; een van de vormen van mucopolysacharidose. | | Morquio syndrome | | Osteochondrodystrophy
Chondro-osteodystrophy
Morquio-Ullrich disease
Morquio disease
Atypical chondrodystrophy
Chondrodystrophia tarda
Hereditary enchondral dysostosis
Familial osseous dystrophy
Keratan sulfaturia
Brailsford-Morquio syndrome
Osteochondrodystrophia deformans
Familial osteochondrodystrophy
Mucopolysaccharidosis type IV
Morquio-Brailsford disease
Mucopolysaccharidosis, MPS-IV
Morquio-Suarez syndrome
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| | DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | E76.2 | | Term | Overige gespecificeerde mucopolysaccharidosen |
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| SNOMED CT to Orphanet simple map | 582 |
| SNOMED CT to MedDRA simple map | 10027983 |
| SNOMED CT to ICD-10 extended map | | Target | E76.2 | | Rule | TRUE | | Advice | ALWAYS E76.2 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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