mannosidosis, nos

Preferred Label : mannosidosis, nos;

Origin ID

D6-72400;

UMLS CUI

C1257960;

Automatic exact mappings (from CISMeF team)
- Defects in glycoprotein degradation [ICD-10 Sub-category (who)]
- Deficiency of alpha-mannosidase (disorder) [SNOMED CT concept]
- alpha-Mannosidosis [MeSH Descriptor]
- alpha-Mannosidosis [MeSH concept]
Currated CISMeF NLP mapping
- Mannosidosis [PASCAL descriptor]
- Mannosidosis [NCIt concept]
- Mannosidosis (disorder) [SNOMED CT concept]
- mannosidase deficiency diseases [MeSH Descriptor]
- mannosidase deficiency diseases [MeSH concept]
- mannosidosis [Disease (Nov.)]
ICD-10 exact mapping(s)
- Defects in glycoprotein degradation [ICD-10 Sub-category (who)]
Metaterm(s)
- metabolism [CISMeF Metaterm]
Référence SNOMED
- alpha-mannosidase [SNOMED Notion]
- congenital deficiency, nos [SNOMED Notion]
SNOMED CT concept
- Mannosidosis (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Mannosidosis [PASCAL descriptor]
- Mannosidosis [NCIt concept]
- Mannosidosis (disorder) [SNOMED CT concept]
- mannosidase deficiency diseases [MeSH concept]
- mannosidase deficiency diseases [MeSH Descriptor]
- mannosidosis [Disease (Nov.)]