atrial fibrillation, familial, 3

Preferred Label : atrial fibrillation, familial, 3;

MeSH note : mutation in KCNQ1;

Origin ID

C563817;

UMLS CUI

C1837014;

Currated CISMeF NLP mapping
- Atrial fibrillation, familial, 3 [OMIM Phenotype]
MeSH term(s) associated for indexing
- atrial fibrillation [MeSH Descriptor]
Record concept(s)
- atrial fibrillation, familial, 3 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Atrial fibrillation, familial, 3 [OMIM Phenotype]