Human Phenotype Ontology 
Grandparent Node:
expandCongestive heart failure (HP:0001635)help
Parent Node:
expandReduced systolic function (HP:0006673)help
..Starting node
..expandGlobal systolic dysfunction (HP:0005185)help
Term ID: 5185
Name: Global systolic dysfunction
Synonym:
Definition: A reduced ejection fraction and an enlarged left ventricle chamber, the latter by an increased resistance to filling with increased filling pressures. Systolic dysfunction is clinically associated with left ventricular failure in the presence of marked cardiomegaly.
Comments:
Reference: HP:0005185
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandImpaired myocardial contractility (HP:0006670) 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:0005185HP:0005185Global systolic dysfunction0 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.