Short qt syndrome 3

Preferred Label : Short qt syndrome 3;

Symbol : SQT3;

CISMeF acronym : SQT3;

Type : Phenotype, molecular basis known;

Prefixed ID : #609622;

Détails

Origin ID

609622;

UMLS CUI

C1865018;

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 3 [MeSH concept]
- short QT syndrome 3 [MeSH Supplementary Concept]
DO Cross reference
- short QT syndrome [DO Concept]
Genes related to phenotype
- Potassium channel, inwardly rectifying, subfamily j, member 2 [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Palpitations [HPO term]
- Shortened QT interval [HPO term]
- Tachycardia [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 3 [MeSH Supplementary Concept]
- short QT syndrome 3 [MeSH concept]

Position du mot-clé dans l'(les) arborescence(s) :

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