congenital sternomastoid torticollis

Preferred Label : congenital sternomastoid torticollis;

Origin ID

D4-B2082;

UMLS CUI

C0079352;

Automatic exact mappings (from CISMeF team)
- Congenital deformity of sternocleidomastoid muscle [ICD-10 Sub-category (who)]
- Congenital torticollis [ICD-11 Category]
- congenital anomaly musculoskeletal [ICPC-2 Rubric]
Currated CISMeF NLP mapping
- Congenital muscular torticollis [HPO term]
- Congenital torticolli [HRDO Sign]
- Congenital torticollis [MeSH concept]
- Congenital torticollis [MedDRA Preferred Term]
- Congenital torticollis (disorder) [SNOMED CT concept]
- Fibromatosis Colli [NCIt concept]
- Fibromatosis colli (disorder) [SNOMED CT concept]
- congenital torticollis [MeSH Supplementary Concept]
ICD-10 exact mapping(s)
- Congenital deformity of sternocleidomastoid muscle [ICD-10 Sub-category (who)]
Metaterm(s)
- pediatrics [CISMeF Metaterm]
Référence SNOMED
- congenital contracture, nos [SNOMED Notion]
- sternocleidomastoid muscle [SNOMED Notion]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital muscular torticollis [HPO term]
- Congenital torticollis [MeSH concept]
- Congenital torticollis [MedDRA Preferred Term]
- Congenital torticollis (disorder) [SNOMED CT concept]
- congenital torticollis [MeSH Supplementary Concept]