mucopolysaccharidosis, mps-i-h/s

Preferred Label : mucopolysaccharidosis, mps-i-h/s;

Origin ID

D6-70116;

UMLS CUI

C0086431;

Currated CISMeF NLP mapping
- Hurler-Scheie Syndrome [NCIt concept]
- Hurler-Scheie syndrome [ORDO Disease]
- Hurler-Scheie syndrome [MedDRA LLT]
- Hurler-Scheie syndrome [MeSH concept]
- Hurler-Scheie syndrome [Disease (Nov.)]
- Hurler-scheie syndrome [OMIM Phenotype]
- Mucopolysaccharidosis IH/S [MedDRA LLT]
- Mucopolysaccharidosis type 1H/S [ICD-11 More detail]
- Mucopolysaccharidosis type I-H/S (disorder) [SNOMED CT concept]
ICD-10 exact mapping(s)
- Mucopolysaccharidosis, type I [ICD-10 Sub-category (who)]
Metaterm(s)
- metabolism [CISMeF Metaterm]
Référence SNOMED
- congenital deficiency, nos [SNOMED Notion]
- l-iduronidase [SNOMED Notion]
SNOMED CT concept
- Mucopolysaccharidosis type I-H/S (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hurler-Scheie Syndrome [NCIt concept]
- Hurler-Scheie syndrome [MedDRA LLT]
- Hurler-Scheie syndrome [ORDO Disease]
- Hurler-Scheie syndrome [MeSH concept]
- Hurler-scheie syndrome [OMIM Phenotype]
- Mucopolysaccharidosis IH/S [MedDRA LLT]
- Mucopolysaccharidosis type 1H/S [ICD-11 More detail]
- Mucopolysaccharidosis type I-H/S (disorder) [SNOMED CT concept]
- mucopolysaccharidosis Ih/s [DO Concept]