Human Phenotype
Ontology
Grandparent Node: Arrhythmia (HP:0011675) Parent Node: Supraventricular arrhythmia (HP:0005115) ..Starting node Atrial standstill (HP:0025478)
Term ID: 25478
Name: Atrial standstill
Synonym: Silent atrium
Definition: Atrial standstill or silent atrium is a rare condition presenting with the absence of electrical and mechanical activity in the atria. It presents with the absence of P waves, bradycardia, and wide QRS complex in the electrocardiogram.
Comments:
Reference: HP:0025478
Genes and Diseases: Child Nodes: Sister Nodes: ..Atrial arrhythmia (HP:0001692) ..Premature atrial contractions (HP:0006699) ..Supraventricular tachycardia (HP:0004755) Input HPO ID HPO term Distance Gene Gene id entrez HGNC ID DiseaseId DiseaseName Frequency Onset HGMD variants ClinVar variants HP:0025478 HP:0025478 Atrial standstill 0 CASQ2 CL E G H 845 1513 OMIM:604772 VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY; CPVT1 129 HP:0025478 HP:0025478 Atrial standstill 0 GJA5 CL E G H 2702 4279 OMIM:108770 Atrial standstill 1 39 HP:0025478 HP:0025478 Atrial standstill 0 NPPA CL E G H 4878 7939 ORPHA:1344 Atrial standstill HP:0040281 - Very frequent 13 HP:0025478 HP:0025478 Atrial standstill 0 NPPA CL E G H 4878 7939 OMIM:615745 Atrial standstill 2 13 HP:0025478 HP:0025478 Atrial standstill 0 RYR2 CL E G H 6262 10484 OMIM:604772 VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY; CPVT1 1103 HP:0025478 HP:0025478 Atrial standstill 0 SCN5A CL E G H 6331 10593 ORPHA:1344 Atrial standstill HP:0040281 - Very frequent 1134 HP:0025478 HP:0025478 Atrial standstill 0 SCN5A CL E G H 6331 10593 OMIM:601154 Cardiomyopathy, dilated, 1E . 1134 HP:0025478 HP:0025478 Atrial standstill 0 TRDN CL E G H 10345 12261 OMIM:604772 VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY; CPVT1 145
Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.
