Craniofacial dysostoses

ICD-11 code : LD25.3;

Preferred Label : Craniofacial dysostoses;

ICD-11 definition : Syndromes caused by abnormal development of skull and facial bones. They may may present with acrocephaly, exophthalmos, hypertelorism, strabismus, parrot-beaked nose, or hypoplastic maxilla. Non-syndromic craniosynostosis, which is predominantly sporadic, is coded elsewhere.;

ICD-11 synonym : Craniofacial dysostosis;

Détails

Origin ID

2114373392;

UMLS CUI

C0010273;

Currated CISMeF NLP mapping
- Craniofacial Dysostosis [NCIt concept]
- Craniofacial dysostosis [MedDRA Preferred Term]
- Craniofacial dysostosis [HPO term]
- Craniofacial dysostosis [ICD-10 Sub-category]
- Crouzon syndrome [DO Concept]
- Crouzon syndrome (disorder) [SNOMED CT concept]
- Dysostosis with predominant craniofacial involvement [ORDO Disease]
- craniofacial dysostosis [MeSH Descriptor]
- craniofacial dysostosis [MeSH concept]
ICD-10 Mapping
- Craniofacial dysostosis [ICD-10 Sub-category]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Craniofacial Dysostosis [NCIt concept]
- Craniofacial dysostosis [HPO term]
- Craniofacial dysostosis [ICD-10 Sub-category]
- Craniofacial dysostosis [MedDRA Preferred Term]
- Crouzon syndrome [DO Concept]
- Crouzon syndrome [ORDO Disease]
- Crouzon syndrome (disorder) [SNOMED CT concept]
- Crouzon's disease [MedDRA LLT]
- Dysostosis with predominant craniofacial involvement [ORDO Disease]
- craniofacial dysostosis [MeSH Descriptor]
- craniofacial dysostosis [MeSH concept]
- crouzon syndrome [SNOMED Notion]

Position du mot-clé dans l'(les) arborescence(s) :

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