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
Nonspherocytic hemolytic anemia (HP:0001930)help
Term ID: 1930
Name: Nonspherocytic hemolytic anemia
Synonym:
Definition:
Comments:
Reference: HP:0001930
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
..expandMicroangiopathic hemolytic anemia (HP:0001937) help
..expandSpontaneous hemolytic crises (HP:0005525) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0001930HP:0001930Nonspherocytic hemolytic anemia0ALDOA CL E G H226611881HNSHA due to aldolase A deficiency611881C0272066OMIM18306414103850
HP:0001930HP:0001930Nonspherocytic hemolytic anemia0BPGM CL E G H669222800Deficiency of bisphosphoglycerate mutase222800C1291620OMIM111371093613896
HP:0001930HP:0001930Nonspherocytic hemolytic anemia0GPI CL E G H2821613470Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency613470C3150730OMIM142454458172400
HP:0001930HP:0001930Nonspherocytic hemolytic anemia0HBA1 CL E G H3039140700Heinz body anemia140700C0700299OMIM12173464823141800
HP:0001930HP:0001930Nonspherocytic hemolytic anemia0HBA2 CL E G H3040140700Heinz body anemia140700C0700299OMIM12962744824141850
HP:0001930HP:0001930Nonspherocytic hemolytic anemia0HBB CL E G H3043140700Heinz body anemia140700C0700299OMIM187110094827141900
HP:0001930HP:0001930Nonspherocytic hemolytic anemia0HK1 CL E G H3098235700Hemolytic anemia due to hexokinase deficiency235700C0472792OMIM19964922142600
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (7) :ALDOA BPGM GPI HBA1 HBA2 HBB HK1

Diseases (5) :611881 222800 613470 140700 235700
 

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