short QT syndrome 1

Preferred Label : short QT syndrome 1;

MeSH note : mutation in KCNH2;

Origin ID

C566506;

UMLS CUI

C1865020;

Currated CISMeF NLP mapping
- Short qt syndrome 1 [OMIM Phenotype]
MeSH term(s) associated for indexing
- arrhythmias, cardiac [MeSH Descriptor]
- heart conduction system [MeSH Descriptor]
- heart defects, congenital [MeSH Descriptor]
Record concept(s)
- short QT syndrome 1 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Short qt syndrome 1 [OMIM Phenotype]
Validated automatic mappings to NTBT
- Short QT Syndrome [NCIt concept]