larsen syndrome

Preferred Label : larsen syndrome;

Origin ID

D4-00815;

UMLS CUI

C0175778;

Automatic exact mappings (from CISMeF team)
- Larsen syndrome [ICD-11 More detail]
- Larsen syndrome [ORDO Disease]
Currated CISMeF NLP mapping
- Larsen syndrome [MedDRA Preferred Term]
- Larsen syndrome [Disease (Nov.)]
- Larsen syndrome [PASCAL descriptor]
- Larsen syndrome [DO Concept]
- Larsen syndrome [OMIM Phenotype]
- Larsen syndrome (disorder) [SNOMED CT concept]
- larsen syndrome [MeSH concept]
- larsen syndrome [MeSH Supplementary Concept]
False automatic mappings
- Orofacial clefting syndrome [ORDO Disease]
ICD-10 exact mapping(s)
- Other specified congenital malformations of limb(s) [ICD-10 Sub-category (who)]
Manual NTBT mappings (CISMeF)
- Primary bone dysplasia with multiple joint dislocations [ORDO Disease]
- Rare developmental defect with connective tissue involvement [ORDO Disease]
Metaterm(s)
- pediatrics [CISMeF Metaterm]
SNOMED CT concept
- Larsen syndrome (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Larsen syndrome [MedDRA Preferred Term]
- Larsen syndrome [OMIM Phenotype]
- Larsen syndrome [Disease (Nov.)]
- Larsen syndrome [DO Concept]
- Larsen syndrome [PASCAL descriptor]
- Larsen syndrome (disorder) [SNOMED CT concept]
- larsen syndrome [MeSH concept]
- larsen syndrome [MeSH Supplementary Concept]