Atrial fibrillation, familial, 4

Preferred Label : Atrial fibrillation, familial, 4;

Symbol : ATFB4;

CISMeF acronym : ATFB4;

Type : Phenotype, molecular basis known;

Prefixed ID : #611493;

Details

Origin ID

611493;

UMLS CUI

C1862394;

Broader ORDO disease(s)
- Familial atrial fibrillation [ORDO Disease]
Currated CISMeF NLP mapping
- atrial fibrillation, familial, 4 [MeSH concept]
- atrial fibrillation, familial, 4 [MeSH Supplementary Concept]
DO Cross reference
- familial atrial fibrillation [DO Concept]
Genes related to phenotype
- Potassium channel, voltage-gated, isk-related subfamily, member 2 [OMIM gene]
HPO term(s)
- Atrial fibrillation [HPO term]
- Autosomal dominant inheritance [HPO term]
- Palpitations [HPO term]
- Paroxysmal atrial fibrillation [HPO term]
- Permanent atrial fibrillation [HPO term]
- Premature atrial contractions [HPO term]
ORDO concept(s)
- Familial atrial fibrillation [ORDO Disease]
See also inter- (CISMeF)
- Familial atrial fibrillation [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- atrial fibrillation, familial, 4 [MeSH Supplementary Concept]
- atrial fibrillation, familial, 4 [MeSH concept]
Validated automatic mappings to NTBT
- familial atrial fibrillation [DO Concept]

Keyword's position in hierarchy(ies) :

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