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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Tachycardia (D013610)
..Starting node ..Atrial Tachyarrhythmia with Short PR Interval (C566237)
Child Nodes:
Sister Nodes:
..Atrial Tachyarrhythmia with Short PR Interval (C566237)
..Bidirectional tachycardia (C535438)
..Tachycardia, Hypertension, Microphthalmia, And Hyperglycinuria (C566880)
..Tachycardia, Paroxysmal (D013614) 1
..Tachycardia, Reciprocating (D054139) 2
..Tachycardia, Supraventricular (D013617) 3
..Tachycardia, Ventricular (D017180) 7
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:

1039

Name:

Atrial Tachyarrhythmia with Short PR Interval

Definition:

Alternative IDs:

ParentIDs:

MESH:D013610

TreeNumbers:

C14.280.067.845/C566237 |C23.550.073.845/C566237

Synonyms:

Slim Mappings:

Cardiovascular disease|Pathology (process)

Reference:

MedGen: C566237
MeSH: C566237
OMIM: 108950;

Genes:

Phenotypes

1	HP:0000006	Autosomal dominant inheritance
2	HP:0004757	Paroxysmal atrial fibrillation
3	HP:0006671	Paroxysmal atrial tachycardia
4	HP:0004754	Permanent atrial fibrillation
5	HP:0005165	Shortened PR interval

Disease Causing ClinVar Variants