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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Microangiopathic hemolytic anemia (HP:0001937)help
Term ID: 1937
Name: Microangiopathic hemolytic anemia
Synonym:
Definition:
Comments:
Reference: HP:0001937
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
..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
..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:0001937HP:0001937Microangiopathic hemolytic anemia0ADAMTS13 CL E G H11093274150Upshaw-Schulman syndrome274150C1268935OMIM11982651366604134
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (1) :ADAMTS13

Diseases (1) :274150
 

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