maroteaux-lamy syndrome, severe form

Preferred Label : maroteaux-lamy syndrome, severe form;

Origin ID

D6-70252;

UMLS CUI

C0268216;

Currated CISMeF NLP mapping
- Maroteaux-Lamy syndrome, severe form (disorder) [SNOMED CT concept]
ICD-10 exact mapping(s)
- Other mucopolysaccharidoses [ICD-10 Sub-category (who)]
Metaterm(s)
- metabolism [CISMeF Metaterm]
Référence SNOMED
- congenital deficiency, nos [SNOMED Notion]
- n-acetylgalactosamine-4-sulfatase [SNOMED Notion]
SNOMED CT concept
- Maroteaux-Lamy syndrome, severe form (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Maroteaux-Lamy syndrome, severe form (disorder) [SNOMED CT concept]