chorea, benign familial

Preferred Label : chorea, benign familial;

Origin ID

C565851;

UMLS CUI

C1859098;

Currated CISMeF NLP mapping
- Benign hereditary chorea [ICD-11 Subcategory]
- Benign hereditary chorea [ORDO Disease]
- Benign hereditary chorea (disorder) [SNOMED CT concept]
- Chorea, benign familial [OMIM Phenotype]
- Chorea, benign hereditary [OMIM Phenotype]
- benign hereditary chorea [Disease (Nov.)]
MeSH term(s) associated for indexing
- chorea [MeSH Descriptor]
Record concept(s)
- chorea, benign familial [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Chorea, benign familial [OMIM Phenotype]