prader-willi syndrome

Preferred Label : prader-willi syndrome;

Origin ID

D4-00615;

UMLS CUI

C0032897;

Currated CISMeF NLP mapping
- Prader Willi syndrome [Disease (Nov.)]
- Prader-Labhart-Willi syndrome [PASCAL descriptor]
- Prader-Willi Syndrome [NCIt concept]
- Prader-Willi syndrome [MedDRA Preferred Term]
- Prader-Willi syndrome [DO Concept]
- Prader-Willi syndrome [ICD-11 Subcategory]
- Prader-Willi syndrome [MeSH concept]
- Prader-Willi syndrome [ICD-9 code]
- Prader-Willi syndrome [ORDO Disease]
- Prader-Willi syndrome (disorder) [SNOMED CT concept]
- Prader-willi syndrome [OMIM Phenotype]
- prader-willi syndrome [MedlinePlus Topic]
- prader-willi syndrome [MeSH Descriptor]
ICD-10 exact mapping(s)
- Congenital malformation syndromes predominantly associated with short stature [ICD-10 Sub-category (who)]
Metaterm(s)
- pediatrics [CISMeF Metaterm]
SNOMED CT concept
- Prader-Willi syndrome (disorder) [SNOMED CT concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Prader Willi syndrome [Disease (Nov.)]
- Prader-Willi Syndrome [NCIt concept]
- Prader-Willi syndrome [ORDO Disease]
- Prader-Willi syndrome [MeSH concept]
- Prader-Willi syndrome [DO Concept]
- Prader-Willi syndrome [ICD-9 code]
- Prader-Willi syndrome [MedDRA Preferred Term]
- Prader-Willi syndrome (disorder) [SNOMED CT concept]
- Prader-willi syndrome [OMIM Phenotype]
- prader-willi syndrome [MeSH Descriptor]
- prader-willi syndrome [MedlinePlus Topic]