Human Phenotype Ontology 
Grandparent Node:
expandAbnormal EKG (HP:0003115)help
Parent Node:
expandAbnormal PR interval (HP:0031593)help
..Starting node
..expandShortened PR interval (HP:0005165)help
Term ID: 5165
Name: Shortened PR interval
Synonym: Electrocardiographic short PR interval; Short P-R interval; Shortened PR interval on EKG
Definition: Reduced time for the PR interval (beginning of the P wave to the beginning of the QRS complex). In adults, normal values are 120 to 200 ms long.
Comments:
Reference: HP:0005165
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandProlonged PR interval (HP:0012248) 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:0005165HP:0005165Shortened PR interval0CACNA1S CL E G H7791397ORPHA:79102Thyrotoxic periodic paralysisHP:0040283 - Occasional247
HP:0005165HP:0005165Shortened PR interval0CYTB CL E G H45197427ORPHA:137675Histiocytoid cardiomyopathyHP:0040284 - Very rare
HP:0005165HP:0005165Shortened PR interval0DOHH CL E G H8347528662OMIM:620066
HP:0005165HP:0005165Shortened PR interval0GAA CL E G H25484065ORPHA:308552Glycogen storage disease due to acid maltase deficiency, infantile onsetHP:0040282 - Frequent407
HP:0005165HP:0005165Shortened PR interval0GAA CL E G H25484065OMIM:232300Glycogen storage disease II.407
HP:0005165HP:0005165Shortened PR interval0GABRA3 CL E G H25564077ORPHA:79102Thyrotoxic periodic paralysisHP:0040283 - Occasional
HP:0005165HP:0005165Shortened PR interval0KCNJ18 CL E G H10013444439080ORPHA:79102Thyrotoxic periodic paralysisHP:0040283 - Occasional10
HP:0005165HP:0005165Shortened PR interval0PRKAG2 CL E G H514229386OMIM:600858Cardiomyopathy, familial hypertrophic, 6235
HP:0005165HP:0005165Shortened PR interval0PRKAG2 CL E G H514229386OMIM:261740Glycogen storage disease of heart, lethal congenital.235
HP:0005165HP:0005165Shortened PR interval0PRKAG2 CL E G H514229386OMIM:194200WOLFF-PARKINSON-WHITE SYNDROME235
HP:0005165HP:0005165Shortened PR interval0TRPM4 CL E G H5479517993OMIM:604559Progressive familial heart block, type IB.124


Genes (8) :CACNA1S CYTB DOHH GAA GABRA3 KCNJ18 PRKAG2 TRPM4

Diseases (9) :ORPHA:79102 ORPHA:137675 OMIM:620066 ORPHA:308552 OMIM:232300 OMIM:600858 OMIM:261740 OMIM:194200 OMIM:604559
 

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