osteogenesis imperfecta, nos

Preferred Label : osteogenesis imperfecta, nos;

Détails

Origin ID

D6-90500;

UMLS CUI

C0029434;

Currated CISMeF NLP mapping
- Brittle bone disease [MedDRA LLT]
- Osteogenesis Imperfecta [NCIt concept]
- Osteogenesis Imperfecta Type I [NCIt concept]
- Osteogenesis imperfecta [MedDRA Preferred Term]
- Osteogenesis imperfecta [PASCAL descriptor]
- Osteogenesis imperfecta [ICD-10 Sub-category]
- Osteogenesis imperfecta [ACR pathology]
- Osteogenesis imperfecta [ACR pathology]
- Osteogenesis imperfecta [ACR pathology]
- Osteogenesis imperfecta [ACR pathology]
- Osteogenesis imperfecta [ICD-11 Sub-sub category]
- Osteogenesis imperfecta [OMIM phenotypic series]
- Osteogenesis imperfecta [ICD-9 code]
- Osteogenesis imperfecta [ICD-10 Sub-category (who)]
- Osteogenesis imperfecta [ORDO Disease]
- Osteogenesis imperfecta (disorder) [SNOMED CT concept]
- Osteogenesis imperfecta type 1 [ICD-11 More detail]
- Osteogenesis imperfecta type 1 [ORDO Disease]
- osteogenesis imperfecta [Radlex concept]
- osteogenesis imperfecta [Disease (Nov.)]
- osteogenesis imperfecta [DO Concept]
- osteogenesis imperfecta [MeSH Descriptor]
- osteogenesis imperfecta [MeSH concept]
- osteogenesis imperfecta [MedlinePlus Topic]
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]
Référence SNOMED
- abnormal bone formation [SNOMED Notion]
- associated with [SNOMED Notion]
- collagen type i [SNOMED Notion]
- defective biosynthesis [SNOMED Notion]
- osteoporosis, nos [SNOMED Notion]
- skeletal system, nos [SNOMED Notion]
SNOMED CT concept
- Osteogenesis imperfecta (disorder) [SNOMED CT concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Brittle bone disease [MedDRA LLT]
- Osteogenesis Imperfecta [NCIt concept]
- Osteogenesis imperfecta [MedDRA Preferred Term]
- Osteogenesis imperfecta [ICD-9 code]
- Osteogenesis imperfecta [ICD-10 Sub-category]
- Osteogenesis imperfecta [ACR pathology]
- Osteogenesis imperfecta [ACR pathology]
- Osteogenesis imperfecta [ACR pathology]
- Osteogenesis imperfecta [ACR pathology]
- Osteogenesis imperfecta [PASCAL descriptor]
- Osteogenesis imperfecta [ICD-11 Sub-sub category]
- Osteogenesis imperfecta [ORDO Disease]
- Osteogenesis imperfecta [ICD-10 Sub-category (who)]
- Osteogenesis imperfecta (disorder) [SNOMED CT concept]
- osteogenesis imperfecta [Radlex concept]
- osteogenesis imperfecta [MeSH concept]
- osteogenesis imperfecta [Disease (Nov.)]
- osteogenesis imperfecta [DO Concept]
- osteogenesis imperfecta [MedlinePlus Topic]
- osteogenesis imperfecta [MeSH Descriptor]
Validated automatic mappings to BTNT
- lobstein's disease [MeSH concept]

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