Human Phenotype Ontology 
Grandparent Node:
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Anemia due to reduced life span of red cells (HP:0011895)help
Parent Node:
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Hemolytic anemia (HP:0001878)help
..Starting node
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Fava bean-induced hemolytic anemia (HP:0004814)help
Term ID: 4814
Name: Fava bean-induced hemolytic anemia
Synonym: Hemolytic anemia following ingestion of fava beans
Definition: A kind of hemolytic anemia that is induced by the ingestion of fava beans.
Comments:
Reference: HP:0004814
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
..expandExercise-induced hemolysis (HP:0005535) 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 entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0004814HP:0004814Fava bean-induced hemolytic anemia0CASK CL E G H8573300908Anemia, nonspherocytic hemolytic, due to G6PD deficiency300908C2720289OMIM11194461497300172
HP:0004814HP:0004814Fava bean-induced hemolytic anemia0G6PD CL E G H2539300908Anemia, nonspherocytic hemolytic, due to G6PD deficiency300908C2720289OMIM12293754057305900
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (2) :CASK G6PD

Diseases (1) :300908
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.