scaphocephaly - CISMeF

Preferred Label : scaphocephaly;

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

Origin ID

M0546050;

UMLS CUI

C0265534;

Automatic exact mappings (from CISMeF team)
- Craniosynostosis [ICD-10 Sub-category (who)]
- Interparietal craniosynostosis (disorder) [SNOMED CT concept]
- Scaphocephaly [ICD-11 More detail]
Currated CISMeF NLP mapping
- Dolichocephaly [ICD-10 Sub-category]
- Dolichocephaly [HPO term]
- Dolichocephaly [MedDRA Preferred Term]
- Dolichocephaly [ICD-10 Sub-category (who)]
- Long narrow head (disorder) [SNOMED CT concept]
- Scaphocephaly [HPO term]
- Scaphocephaly [MedDRA Preferred Term]
- Scaphycephaly (disorder) [Inactive SNOMED CT concept]
- dolichocephaly [SNOMED Notion]
- scaphocephaly [SNOMED Notion]
- scaphocephaly [Radlex concept]
Manual BTNT mappings - CISMeF
- Familial scaphocephaly syndrome, McGillivray type [ORDO Disease]
- Non-syndromic sagittal craniosynostosis [ORDO Disease]
Related record
- craniosynostoses [MeSH Descriptor]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Non-syndromic sagittal craniosynostosis [ORDO Disease]
- Scaphocephaly [MedDRA Preferred Term]
- Scaphocephaly [HPO term]
- Scaphycephaly (disorder) [Inactive SNOMED CT concept]
- scaphocephaly [SNOMED Notion]