leri-weill dyschondrosteosis

Preferred Label : leri-weill dyschondrosteosis;

Details

Origin ID

D4-00D07;

UMLS CUI

C0265309;

Currated CISMeF NLP mapping
- Leri Weill dyschondrosteosis [Disease (Nov.)]
- Leri-Weil syndrome [MeSH concept]
- Leri-Weil syndrome [MeSH Supplementary Concept]
- Leri-Weill Dyschondrosteosis [NCIt concept]
- Leri-Weill dyschondrosteosis [DO Concept]
- Leri-Weill dyschondrosteosis (disorder) [SNOMED CT concept]
- Leri-Weill syndrome [MedDRA LLT]
- Leri-weill dyschondrosteosis [OMIM Phenotype]
- Léri-Weill dyschondrosteosis [ICD-11 More detail]
- Léri-Weill dyschondrosteosis [ORDO Disease]
ICD-10 exact mapping(s)
- Other specified osteochondrodysplasias [ICD-10 Sub-category (who)]
Manual NTBT mappings (CISMeF)
- Chondrodysplastic malformation syndrome [ORDO Disease]
- Mesomelic and rhizo-mesomelic dysplasia [ORDO Disease]
Metaterm(s)
- pediatrics [CISMeF Metaterm]
SNOMED CT concept
- Leri-Weill dyschondrosteosis (disorder) [SNOMED CT concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Dyschondrosteosis [MedDRA Preferred Term]
- Leri Weill dyschondrosteosis [Disease (Nov.)]
- Leri-Weil syndrome [MeSH Supplementary Concept]
- Leri-Weil syndrome [MeSH concept]
- Leri-Weill Dyschondrosteosis [NCIt concept]
- Leri-Weill dyschondrosteosis [DO Concept]
- Leri-Weill dyschondrosteosis (disorder) [SNOMED CT concept]
- Leri-Weill syndrome [MedDRA LLT]
- Leri-weill dyschondrosteosis [OMIM Phenotype]
- Léri-Weill dyschondrosteosis [ORDO Disease]
- Léri-Weill dyschondrosteosis [ICD-11 More detail]

Keyword's position in hierarchy(ies) :

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