Human Phenotype Ontology 
Grandparent Node:
expandAbnormal cardiac test (HP:0500015)help
Grandparent Node:
expandAbnormality of cardiovascular system electrophysiology (HP:0030956)help
Parent Node:
expandAbnormal EKG (HP:0003115)help
..Starting node
..expandAbnormal PR segment (HP:0031596)help
Term ID: 31596
Name: Abnormal PR segment
Synonym:
Definition: An anomaly of the PR segment, which begins at the endpoint of the P wave and ends at the onset of the QRS complex. The PR segment is normally flat and isoelectric.
Comments:
Reference: HP:0031596
Genes and Diseases:
 
       Child Nodes:
........expandPR segment depression (HP:0031594) help
........expandPR segment elevation (HP:0031597) help

 Sister Nodes: 
..expandAbnormal P wave (HP:0031595) help
..expandAbnormal PR interval (HP:0031593) help
..expandAbnormal QRS complex (HP:0025074) help
..expandAbnormal QT interval (HP:0031547) help
..expandAbnormal ST segment (HP:0012249) help
..expandAbnormal T-wave (HP:0005135) help
..expandAbnormal U wave (HP:0025070) help
..expandJ wave (HP:0012272) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031596HP:0031596Abnormal PR segment0 CL E G H
HP:0031596HP:0031597PR segment elevation1 CL E G H
HP:0031596HP:0031594PR segment depression1 CL E G H


Genes (0) :

Diseases (0) :
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.