Ventricular fibrillation, paroxysmal familial, 1

Preferred Label : Ventricular fibrillation, paroxysmal familial, 1;

Symbol : VF1;

CISMeF acronym : IVF; VF; VF1;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : VF; IVF;

Included titles and symbols : Ventricular fibrillation during myocardial infarction, susceptibility to;

Prefixed ID : #603829;

Details

Origin ID

603829;

UMLS CUI

C2751898;

Automatic exact mappings (from CISMeF team)
- FIBRILLATION VENTRICULAR [WHO-ART Preferred Term]
- Idiopathic ventricular fibrillation, non Brugada type [ORDO Disease]
- In Vitro Fertilization [NCIt concept]
- NAMPT wt Allele [NCIt concept]
- Per Visual Field [NCIt concept]
- SCN5A wt Allele [NCIt concept]
- Test tube ovum fertilization (procedure) [SNOMED CT concept]
- Ventricular Fibrillation [NCIt concept]
- Ventricular Fibrillation by ECG Finding [NCIt concept]
- Ventricular fibrillation [MedDRA Preferred Term]
- assisted reproductive technology [MedlinePlus Topic]
- fertilization in vitro [MeSH Descriptor]
- sodium voltage-gated channel alpha subunit 5 [ORDO Gene]
- ventricular fibrillation [MeSH Descriptor]
- ventricular fibrillation [SNOMED Notion]
- ventricular fibrillation [MeSH concept]
Currated CISMeF NLP mapping
- ventricular fibrillation, paroxysmal familial, 1 [MeSH concept]
- ventricular fibrillation, paroxysmal familial, 1 [MeSH Supplementary Concept]
Genes related to phenotype
- Sodium voltage-gated channel, alpha subunit 5 [OMIM gene]
HPO term(s)
- Syncope [HPO term]
- Tachycardia [HPO term]
- Ventricular fibrillation [HPO term]
ORDO concept(s)
- Idiopathic ventricular fibrillation, non Brugada type [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- ventricular fibrillation, paroxysmal familial, 1 [MeSH Supplementary Concept]
- ventricular fibrillation, paroxysmal familial, 1 [MeSH concept]

Keyword's position in hierarchy(ies) :

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