Short qt syndrome 1

Preferred Label : Short qt syndrome 1;

Symbol : SQT1;

CISMeF acronym : SQT1;

Type : Phenotype, molecular basis known;

Prefixed ID : #609620;

Details

Origin ID

609620;

UMLS CUI

C1865020;

Automatic exact mappings (from CISMeF team)
- Familial short QT syndrome [ORDO Disease]
Broader ORDO disease(s)
- Familial short QT syndrome [ORDO Disease]
Currated CISMeF NLP mapping
- short QT syndrome 1 [MeSH concept]
- short QT syndrome 1 [MeSH Supplementary Concept]
DO Cross reference
- short QT syndrome [DO Concept]
Genes related to phenotype
- Potassium channel, voltage-gated, subfamily h, member 2 [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Cardiac arrest [HPO term]
- Palpitations [HPO term]
- Paroxysmal atrial fibrillation [HPO term]
- Shortened QT interval [HPO term]
- Sudden cardiac death [HPO term]
- Syncope [HPO term]
ORDO concept(s)
- Familial short QT syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- short QT syndrome 1 [MeSH Supplementary Concept]
- short QT syndrome 1 [MeSH concept]

Keyword's position in hierarchy(ies) :

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