osteogenesis imperfecta with blue sclerae

Preferred Label : osteogenesis imperfecta with blue sclerae;

Details

Origin ID

D6-90510;

UMLS CUI

C0023931;

Automatic exact mappings (from CISMeF team)
- van de Hoeve syndrome (disorder) [Inactive SNOMED CT concept]
CISMeF manual mappings
- Osteogenesis imperfecta [ORDO Disease]
- Osteogenesis imperfecta type I (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Brittle bone disease [MedDRA LLT]
- Osteogenesis Imperfecta [NCIt concept]
- Osteogenesis Imperfecta Type I [NCIt concept]
- Osteogenesis Imperfecta, type I [OMIM Phenotype]
- Osteogenesis imperfecta [OMIM phenotypic series]
- Osteogenesis imperfecta [ICD-10 Sub-category]
- Osteogenesis imperfecta [ICD-9 code]
- Osteogenesis imperfecta [ACR pathology]
- Osteogenesis imperfecta [MedDRA Preferred Term]
- Osteogenesis imperfecta [ACR pathology]
- Osteogenesis imperfecta [ACR pathology]
- Osteogenesis imperfecta [ICD-11 Sub-sub category]
- Osteogenesis imperfecta [ACR pathology]
- Osteogenesis imperfecta [ICD-10 Sub-category (who)]
- Osteogenesis imperfecta [PASCAL descriptor]
- Osteogenesis imperfecta (disorder) [SNOMED CT concept]
- Osteogenesis imperfecta type 1 [ORDO Disease]
- Osteogenesis imperfecta type 1 [ICD-11 More detail]
- lobstein's disease [MeSH concept]
- osteogenesis imperfecta [Disease (Nov.)]
- osteogenesis imperfecta [MeSH Descriptor]
- osteogenesis imperfecta [MeSH concept]
- osteogenesis imperfecta [Radlex concept]
- osteogenesis imperfecta [DO Concept]
- osteogenesis imperfecta [MedlinePlus Topic]
- osteogenesis imperfecta type 1 [DO Concept]
- van der Hoeve syndrome [Disease (Nov.)]
ICD-10 exact mapping(s)
- Osteogenesis imperfecta [ICD-10 Sub-category (who)]
Manual BTNT mappings - CISMeF
- Osteogenesis imperfecta type 2 [ORDO Disease]
- Osteogenesis imperfecta type 3 [ORDO Disease]
- Osteogenesis imperfecta type 4 [ORDO Disease]
- Osteogenesis imperfecta type 5 [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Primary bone dysplasia with decreased bone density [ORDO Disease]
Metaterm(s)
- metabolism [CISMeF Metaterm]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Osteogenesis Imperfecta Type I [NCIt concept]
- Osteogenesis Imperfecta, type I [OMIM Phenotype]
- Osteogenesis imperfecta type I (disorder) [SNOMED CT concept]
- lobstein's disease [MeSH concept]
- osteogenesis imperfecta type 1 [DO Concept]
- van der Hoeve syndrome [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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