Arnold-Chiari malformation, type I

Preferred Label : Arnold-Chiari malformation, type I;

UMLS semantic type : T019 - Congenital Abnormality;

Origin ID

M0336996;

UMLS CUI

C0750929;

Automatic exact mappings (from CISMeF team)
- Arnold-Chiari malformation type I [ICD-11 Subcategory]
Currated CISMeF NLP mapping
- Arnold-Chiari malformation type I [ORDO Disease]
- Arnold-Chiari malformation type I [MedDRA LLT]
- Chiari malformation type I [OMIM Phenotype]
- Chiari malformation type I [Disease (Nov.)]
- Chiari malformation type I (disorder) [SNOMED CT concept]
- Chiari type I malformation [HPO term]
- chiari malformation type I [Radlex concept]
Related record
- arnold-chiari malformation [MeSH Descriptor]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Arnold-Chiari malformation type I [MedDRA LLT]
- Arnold-Chiari malformation type I [ORDO Disease]
- Chiari malformation type I [OMIM Phenotype]
- Chiari malformation type I [Disease (Nov.)]
- Chiari malformation type I (disorder) [SNOMED CT concept]
- Chiari type I malformation [HPO term]
- chiari malformation type I [Radlex concept]