cortical defects, wormian bones, and dentinogenesis imperfecta

Preferred Label : cortical defects, wormian bones, and dentinogenesis imperfecta;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0566034;

UMLS CUI

C1858032;

Currated CISMeF NLP mapping
- Cortical defects, wormian bones, and dentinogenesis imperfecta [OMIM Phenotype]
- Skeletal dysplasia with wormian bone, multiple fractures, dentinogenesis imperfecta syndrome (disorder) [SNOMED CT concept]
- Wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia [ORDO Disease]
Related record
- cortical defects, wormian bones, and dentinogenesis imperfecta [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cortical defects, wormian bones, and dentinogenesis imperfecta [OMIM Phenotype]
- Wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia [ORDO Disease]