Human Phenotype Ontology 
Grandparent Node:
expandAnemia due to reduced life span of red cells (HP:0011895)help
Parent Node:
expandHemolytic anemia (HP:0001878)help
..Starting node
..expandExercise-induced hemolysis (HP:0005535)help
Term ID: 5535
Name: Exercise-induced hemolysis
Synonym:
Definition: A form of hemolytic anemia that can be triggered by exertion.
Comments:
Reference: HP:0005535
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAutoimmune hemolytic anemia (HP:0001890) help
..expandChronic hemolytic anemia (HP:0004870) help
..expandCold-induced hemolysis (HP:0031484) help
..expandCompensated hemolytic anemia (HP:0004863) help
..expandCongenital hemolytic anemia (HP:0004804) help
..expandCoombs-positive hemolytic anemia (HP:0004844) help
..expandDrug-sensitive hemolytic anemia (HP:0004817) help
..expandEpisodic hemolytic anemia (HP:0004802) help
..expandFava bean-induced hemolytic anemia (HP:0004814) help
..expandHeinz body anemia (HP:0005511) help
..expandIncreased red cell hemolysis by shear stress (HP:0008269) help
..expandMacrocytic hemolytic disease (HP:0005524) help
..expandMicroangiopathic hemolytic anemia (HP:0001937) help
..expandNonspherocytic hemolytic anemia (HP:0001930) help
..expandSpontaneous hemolytic crises (HP:0005525) 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:0005535HP:0005535Exercise-induced hemolysis0PIEZO1 CL E G H978028993OMIM:194380Dehydrated hereditary stomatocytosis 1 with or without pseudohyperkalemia and/or perinatal edema.36


Genes (1) :PIEZO1

Diseases (1) :OMIM:194380
 

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