Atrial fibrillation, familial, 8

Preferred Label : Atrial fibrillation, familial, 8;

Symbol : ATFB8;

CISMeF acronym : ATFB8;

Type : Phenotype, molecular basis known;

Description : For a phenotypic description and a discussion of genetic heterogeneity of atrial fibrillation, see 608583.;

Prefixed ID : #613055;

Details

Origin ID

613055;

UMLS CUI

C2751607;

Broader ORDO disease(s)
- Familial atrial fibrillation [ORDO Disease]
Currated CISMeF NLP mapping
- atrial fibrillation, familial, 8 [MeSH concept]
- atrial fibrillation, familial, 8 [MeSH Supplementary Concept]
DO Cross reference
- familial atrial fibrillation [DO Concept]
Genes related to phenotype
- Zinc finger homeobox 3 [OMIM gene]
ORDO concept(s)
- Familial atrial fibrillation [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- atrial fibrillation, familial, 8 [MeSH Supplementary Concept]
- atrial fibrillation, familial, 8 [MeSH concept]
Validated automatic mappings to NTBT
- familial atrial fibrillation [DO Concept]

Keyword's position in hierarchy(ies) :

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