Atrial standstill 1

Preferred Label : Atrial standstill 1;

Symbol : ATRST1;

CISMeF acronym : ATRST1;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Atrial cardiomyopathy with heart block; Cardiomyopathy, familial, with conduction disturbance;

Inheritance : Autosomal dominant;

Prefixed ID : #108770;

Details

Origin ID

108770;

UMLS CUI

C4551959;

Automatic exact mappings (from CISMeF team)
- atrial standstill 1 [DO Concept]
Currated CISMeF NLP mapping
- Atrial standstill [HPO term]
- Atrial standstill [ORDO Disease]
- Atrial standstill (disorder) [SNOMED CT concept]
- atrial standstill [Disease (Nov.)]
- atrial standstill [MeSH concept]
- atrial standstill [MeSH Supplementary Concept]
DO Cross reference
- atrial standstill 1 [DO Concept]
Genes related to phenotype
- Gap junction protein, alpha-5 [OMIM gene]
HPO term(s)
- Atrial cardiomyopathy [HPO term]
- Atrial standstill [HPO term]
- Autosomal dominant inheritance [HPO term]
- Endocardial fibroelastosis [HPO term]
- First degree atrioventricular block [HPO term]
- Heart block [HPO term]
- Paroxysmal atrial fibrillation [HPO term]
- Premature atrial contractions [HPO term]
- Ventricular escape rhythm [HPO term]
ORDO concept(s)
- Atrial standstill [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Atrial standstill [ORDO Disease]
- atrial standstill [MeSH Supplementary Concept]
- atrial standstill [MeSH concept]

Keyword's position in hierarchy(ies) :

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