Human Phenotype
Ontology
Grandparent Node: Abnormal EKG (HP:0003115) Parent Node: Abnormal QRS complex (HP:0025074) ..Starting node .. Prolonged QRS complex (HP:0006677)
Term ID:
6677
Name:
Prolonged QRS complex
Synonym:
Intraventricular conduction delay; Prolonged QRS complex on EKG; QRS widening
Definition:
Increased time for the complex comprised of the Q wave, R wave, and S wave as measured by the electrocardiogram (EKG).. In adults, normal values are 0.06 - 0.10 sec.
Comments:
Reference:
HP:0006677
Genes and Diseases: Child Nodes: Sister Nodes: ..Abnormal QRS voltage (HP:0025076) Input HPO ID HPO term Distance Gene Gene id entrez HGNC ID DiseaseId DiseaseName Frequency Onset HGMD variants ClinVar variants HPO disease - gene - phenotype typical associations: HPO disease - gene - phenotype less frequent non-typical associations: HP:0006677 HP:0006677 Prolonged QRS complex 0 GJA5 CL E G H 2702 4279 OMIM:614049 Atrial fibrillation, familial, 11 39 HP:0006677 HP:0006677 Prolonged QRS complex 0 IRX5 CL E G H 10265 14361 OMIM:611174 Hamamy syndrome 4 HP:0006677 HP:0006677 Prolonged QRS complex 0 JUP CL E G H 3728 6207 OMIM:611528 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 12; ARVD12 222 HP:0006677 HP:0006677 Prolonged QRS complex 0 JUP CL E G H 3728 6207 OMIM:601214 Naxos disease 222 HP:0006677 HP:0006677 Prolonged QRS complex 0 PKP2 CL E G H 5318 9024 OMIM:609040 Arrhythmogenic right ventricular dysplasia, familial, 9 406 HP:0006677 HP:0006677 Prolonged QRS complex 0 PRKAG2 CL E G H 51422 9386 OMIM:600858 Cardiomyopathy, familial hypertrophic, 6 235 HP:0006677 HP:0006677 Prolonged QRS complex 0 PRKAG2 CL E G H 51422 9386 OMIM:194200 WOLFF-PARKINSON-WHITE SYNDROME 235 HP:0006677 HP:0006677 Prolonged QRS complex 0 TMEM43 CL E G H 79188 28472 OMIM:604400 Arrhythmogenic right ventricular dysplasia, familial, 5 171
Genes (6) :GJA5 IRX5 JUP PKP2 PRKAG2 TMEM43 Diseases (8) :OMIM:614049 OMIM:611174 OMIM:611528 OMIM:601214 OMIM:609040 OMIM:600858 OMIM:194200 OMIM:604400
Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.