Atrial fibrillation, familial, 2

Preferred Label : Atrial fibrillation, familial, 2;

Symbol : ATFB2;

CISMeF acronym : ATFB2;

Type : Phenotype or locus, molecular basis unknown;

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

Prefixed ID : %608988;

Details

Origin ID

608988;

UMLS CUI

C1837812;

Broader ORDO disease(s)
- Familial atrial fibrillation [ORDO Disease]
Currated CISMeF NLP mapping
- atrial fibrillation, familial, 2 [MeSH concept]
- atrial fibrillation, familial, 2 [MeSH Supplementary Concept]
DO Cross reference
- familial atrial fibrillation [DO Concept]
ORDO concept(s)
- Familial atrial fibrillation [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- atrial fibrillation, familial, 2 [MeSH Supplementary Concept]
- atrial fibrillation, familial, 2 [MeSH concept]
Validated automatic mappings to NTBT
- familial atrial fibrillation [DO Concept]

Keyword's position in hierarchy(ies) :

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