Osteogenesis imperfecta, type 1A

Preferred Label : Osteogenesis imperfecta, type 1A;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0530502;

UMLS CUI

C0268357;

Automatic exact mappings (from CISMeF team)
- Osteogenesis imperfecta with blue sclerae AND dentinogenesis imperfecta (disorder) [SNOMED CT concept]
Related record
- osteogenesis imperfecta, type 1A [MeSH Supplementary Concept]
See also inter- (CISMeF)
- Dentinogenesis imperfecta - Shield's type I (disorder) [SNOMED CT concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Dentinogenesis imperfecta - Shield's type I (disorder) [SNOMED CT concept]
- Dentinogenesis imperfecta, osteogenesis imperfecta [ACR pathology]
- Osteogenesis imperfecta with blue sclerae AND dentinogenesis imperfecta (disorder) [SNOMED CT concept]
- dentinogenesis imperfecta type I [Disease (Nov.)]
- osteogenesis imperfecta with blue sclerae and dentinogenesis imperfecta [SNOMED Notion]