craniofacial dysostosis

Preferred Label : craniofacial dysostosis;

UMLS semantic type : T019 - Congenital Abnormality; T047 - Disease or Syndrome;

Origin ID

M0005284;

UMLS CUI

C0010273;

Currated CISMeF NLP mapping
- Craniofacial Dysostosis [NCIt concept]
- Craniofacial dysostoses [ICD-11 Subcategory]
- Craniofacial dysostosis [ICD-10 Sub-category]
- Craniofacial dysostosis [ICD-10 Sub-category (who)]
- Craniofacial dysostosis [HPO term]
- Craniofacial dysostosis [MedDRA Preferred Term]
- Crouzon disease [PASCAL descriptor]
- Crouzon disease [ICD-11 Sub-sub category]
- Crouzon syndrome [Disease (Nov.)]
- Crouzon syndrome [DO Concept]
- Crouzon syndrome [ORDO Disease]
- Crouzon syndrome [OMIM Phenotype]
- Crouzon syndrome (disorder) [SNOMED CT concept]
- Crouzon's disease [MedDRA LLT]
- Dysostosis with predominant craniofacial involvement [ORDO Disease]
- crouzon syndrome [SNOMED Notion]
MeSH narrower concept(s)
- crouzon disease [MeSH concept]
Related record
- craniofacial dysostosis [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Craniofacial Dysostosis [NCIt concept]
- Craniofacial dysostoses [ICD-11 Subcategory]
- Craniofacial dysostosis [ICD-10 Sub-category]
- Craniofacial dysostosis [HPO term]
- Craniofacial dysostosis [ICD-10 Sub-category (who)]
- Craniofacial dysostosis [MedDRA Preferred Term]
- Crouzon syndrome [ORDO Disease]
- Crouzon syndrome [DO Concept]
- Crouzon syndrome (disorder) [SNOMED CT concept]
- Crouzon's disease [MedDRA LLT]
- Dysostosis with predominant craniofacial involvement [ORDO Disease]
- crouzon syndrome [SNOMED Notion]