{"orpha":98372,"name":"Hemolytic anemia due to a disorder of glycolytic enzymes","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"definition":null,"note":"This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.","url":"https://raremap.alftech.space/d/ORPHA-98372/","orphanet_url":"https://www.orpha.net/en/disease/detail/98372","names":{"fr":{"name":"Anémie hémolytique par anomalie des enzymes glycolytiques"},"de":{"name":"Hämolytische Anämie infolge einer Störung der glykolytischen Enzyme"},"es":{"name":"Anemia hemolítica por anomalías de las enzimas glicolíticas"},"it":{"name":"Anemia emolitica da difetti degli enzimi glicolitici"},"nl":{"name":"Hemolytische anemie als gevolg van een stoornis van glycolytische enzymen"},"pt":{"name":"Doença glicolítica"},"pl":{"name":"Niedokrwistość hemolityczna z powodu zaburzeń enzymów glikolitycznych"},"cs":{"name":"Hemolytická anémie způsobená poruchou enzymů glykolýzy"},"uk":{"name":"Гемолітична анемія внаслідок порушення гліколітичних ферментів"},"zh":{"name":"糖酵解酶异常所致溶血性贫血"},"tr":{"name":"Glikolitik enzim bozukluğuna bağlı hemolitik anemi"}},"xrefs":[{"source":"ICD-10","code":"D55.2","qualifier":"E","icd_relation":"specific","validated":true},{"source":"ICD-11","code":"3A10.Y","qualifier":"NTBT","icd_relation":"index","validated":true,"icd11_uri":"265398117"},{"source":"UMLS","code":"C5681713","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":248305,"name":"OBSOLETE: Hemolytic anemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency","status":"inactive"}],"preferential_parent":{"orpha":97992,"name":"Rare hematologic disease"},"parents":[{"orpha":98369,"name":"Rare constitutional hemolytic anemia due to an enzyme disorder","classifications":[156,194]}],"children":[{"orpha":466026,"name":"Class I glucose-6-phosphate dehydrogenase deficiency","type":"Disease"},{"orpha":57,"name":"Glycogen storage disease due to aldolase A deficiency","type":"Disease"},{"orpha":371,"name":"Glycogen storage disease due to muscle phosphofructokinase deficiency","type":"Disease"},{"orpha":713,"name":"Glycogen storage disease due to phosphoglycerate kinase 1 deficiency","type":"Disease"},{"orpha":714,"name":"Hemolytic anemia due to diphosphoglycerate mutase deficiency","type":"Disease"},{"orpha":712,"name":"Hemolytic anemia due to glucophosphate isomerase deficiency","type":"Disease"},{"orpha":766,"name":"Hemolytic anemia due to red cell pyruvate kinase deficiency","type":"Disease"},{"orpha":90031,"name":"Non-spherocytic hemolytic anemia due to hexokinase deficiency","type":"Disease"},{"orpha":868,"name":"Triose phosphate-isomerase deficiency","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}