Human Phenotype Ontology 
Grandparent Node:
expandAbnormal thrombosis (HP:0001977)help
Parent Node:
expandThromboembolism (HP:0001907)help
..Starting node
..expandRecurrent thromboembolism (HP:0004831)help
Term ID: 4831
Name: Recurrent thromboembolism
Synonym: Recurrent thromboembolic disease
Definition: Repeated episodes of obstruction of blood flow due to an embolus, i.e., blood clot that has traveled from its point of origin within the blood stream.
Comments:
Reference: HP:0004831
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandThromboembolic stroke (HP:0001727) 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:0004831HP:0004831Recurrent thromboembolism0HRG CL E G H32735181OMIM:613116Thrombophilia due to histidine-rich glycoprotein deficiency.4
HP:0004831HP:0004831Recurrent thromboembolism0SERPINC1 CL E G H462775ORPHA:82Hereditary thrombophilia due to congenital antithrombin deficiencyHP:0040282 - Frequent88


Genes (2) :HRG SERPINC1

Diseases (2) :OMIM:613116 ORPHA:82
 

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