Human Phenotype Ontology 
Grandparent Node:
expand
Anemia due to reduced life span of red cells (HP:0011895)help
Parent Node:
expand
Hemolytic anemia (HP:0001878)help
..Starting node
..expand
Drug-sensitive hemolytic anemia (HP:0004817)help
Term ID: 4817
Name: Drug-sensitive hemolytic anemia
Synonym: Drug-sensitive hemolytic anaemia
Definition: A form of hemolytic anemia that is triggered by ingestion of certain drugs.
Comments:
Reference: HP:0004817
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
..expandEpisodic hemolytic anemia (HP:0004802) help
..expandExercise-induced hemolysis (HP:0005535) 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:0004817HP:0004817Drug-sensitive hemolytic anemia0HBB CL E G H30434827ORPHA:2133Hemoglobin E diseaseHP:0040283 - Occasional580


Genes (1) :HBB

Diseases (1) :ORPHA:2133
 

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