niemann-pick disease, type d

Preferred Label : niemann-pick disease, type d;

Origin ID

D6-74040;

UMLS CUI

C0268247;

Automatic exact mappings (from CISMeF team)
- Niemann-Pick disease, nova scotian type [MeSH concept]
- Niemann-Pick disease, nova scotian type [MeSH Supplementary Concept]
- Niemann-Pick disease, type A [MeSH Descriptor]
- Niemann-pick disease, type c1 [OMIM Phenotype]
- niemann-pick diseases [MeSH Descriptor]
Currated CISMeF NLP mapping
- Niemann Pick disease type D [Disease (Nov.)]
- Niemann-Pick disease type D [ORDO Disease]
- Niemann-Pick disease, type D [MeSH concept]
- Niemann-Pick disease, type D (disorder) [SNOMED CT concept]
False automatic mappings
- Niemann-Pick disease, type B [MeSH Descriptor]
ICD-10 exact mapping(s)
- Other sphingolipidosis [ICD-10 Sub-category (who)]
Metaterm(s)
- metabolism [CISMeF Metaterm]
Référence SNOMED
- congenital deficiency, nos [SNOMED Notion]
- sphingomyelin phosphodiesterase [SNOMED Notion]
SNOMED CT concept
- Niemann-Pick disease, type D (disorder) [SNOMED CT concept]
See also inter- (CISMeF)
- Niemann-Pick Disease, Type C [NCIt concept]
- Niemann-Pick disease type C [ICD-11 More detail]
- Niemann-Pick disease, type C [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Niemann-Pick disease type D [ORDO Disease]
- Niemann-Pick disease, type D [MeSH concept]
- Niemann-Pick disease, type D (disorder) [SNOMED CT concept]