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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Chronic hemolytic anemia (HP:0004870)help
Term ID: 4870
Name: Chronic hemolytic anemia
Synonym: hemolytic anemia, chronic
Definition: An chronic form of hemolytic anemia.
Comments:
Reference: HP:0004870
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAutoimmune hemolytic anemia (HP:0001890) 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
..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 entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0004870HP:0004870Chronic hemolytic anemia0ABCG5 CL E G H64240210250Sitosterolemia210250C0342907OMIM14720113886605459
HP:0004870HP:0004870Chronic hemolytic anemia0ABCG8 CL E G H64241210250Sitosterolemia210250C0342907OMIM15129313887605460
HP:0004870HP:0004870Chronic hemolytic anemia0HBB CL E G H3043232Medullary sponge kidneyORPHA187110094827141900
HP:0004870HP:0004870Chronic hemolytic anemia0NHLRC2 CL E G H374354618278618278618278OMIM1228247310
HP:0004870HP:0004870Chronic hemolytic anemia0PKLR CL E G H5313766ORPHA12821199020609712
HP:0004870HP:0004870Chronic hemolytic anemia0PKLR CL E G H5313266200Pyruvate kinase deficiency of red cells266200C0340968OMIM12821199020609712
HP:0004870HP:0004870Chronic hemolytic anemia0TPI1 CL E G H7167615512Triosephosphate isomerase deficiency615512C1860808OMIM11910412009190450
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (6) :ABCG5 ABCG8 HBB NHLRC2 PKLR TPI1

Diseases (6) :210250 232 618278 766 266200 615512
 

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