Platyspondyly - amelogenesis imperfecta - CISMeF

" /> Platyspondyly - amelogenesis imperfecta - CISMeF

CISMeF

chu

Platyspondyly - amelogenesis imperfectaICD-11 More detail

Preferred Label : Platyspondyly - amelogenesis imperfecta;

Details

Origin ID

792334455;

UMLS CUI

C1832594;

Currated CISMeF NLP mapping
- Autosomal recessive brachyolmia and amelogenesis imperfecta syndrome (disorder) [SNOMED CT concept]
- Brachyolmia-amelogenesis imperfecta syndrome [ORDO Disease]
- Dental anomalies and short stature [OMIM Phenotype]
- Verloes Bourguignon syndrome [MeSH concept]
- brachyolmia-amelogenesis imperfecta syndrome [DO Concept]
- verloes bourguignon syndrome [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal recessive brachyolmia and amelogenesis imperfecta syndrome (disorder) [SNOMED CT concept]
- Brachyolmia-amelogenesis imperfecta syndrome [ORDO Disease]
- Brachyolmia-amelogenesis imperfecta syndrome [MedDRA LLT]
- Dental anomalies and short stature [OMIM Phenotype]
- Verloes Bourguignon syndrome [MeSH concept]
- brachyolmia-amelogenesis imperfecta syndrome [DO Concept]
- verloes bourguignon syndrome [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients

Nous contacter.
04/05/2025

© Rouen University Hospital. Any partial or total use of this material must mention the source.