{"orpha":98374,"name":"Hemolytic anemia due to an erythrocyte nucleotide metabolism disorder","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":["Hemolytic anemia due to an erythroenzymopathy"],"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-98374/","orphanet_url":"https://www.orpha.net/en/disease/detail/98374","names":{"fr":{"name":"Anémie hémolytique par anomalie du métabolisme nucléotidique de l'érythrocyte","synonyms":["Anémie hémolytique par erythroenzymopathie"]},"de":{"name":"Hämolytische Anämie durch Erythrozyten-Nukleotidstoffwechselstörung","synonyms":["Hämolytische Anämie durch Erythroenzymopathie"]},"es":{"name":"Anemia hemolítica por trastorno del metabolismo nucleotídico de los eritrocitos","synonyms":["Anemia hemolítica por una eritroenzimopatía"]},"it":{"name":"Anemia emolitica da difetto del metabolismo nucleotidico degli eritrociti","synonyms":["Anemia emolitica da eritroenzimopatia"]},"nl":{"name":"Hemolytische anemie als gevolg van een erytrocytnucleotidestofwisselingsstoornis","synonyms":["Hemolytische anemie als gevolg van een erytro-enzymopathie"]},"pt":{"name":"Doença do metabolismo nucleotídico dos eritrócitos"},"pl":{"name":"Niedokrwistość hemolityczna z powodu zaburzeń metabolizmu nukleotydów w erytrocytach","synonyms":["Niedokrwistość hemolityczna z powodu erytroenzymopatii"]},"cs":{"name":"Hemolytická anémie způsobená poruchou metabolismu nukleotidů erytrocytu","synonyms":["Hemolytická anémie způsobená enzymopatií erytrocytů"]},"uk":{"name":"Гемолітична анемія внаслідок порушення нуклеотидного обміну еритроцитів","synonyms":["Гемолітична анемія внаслідок еритроензимопатії"]},"zh":{"name":"红细胞核苷酸代谢紊乱所致溶血性贫血","synonyms":["红细胞酶病所致溶血性贫血"]},"tr":{"name":"Eritrosit nükleotid metabolizması bozukluğuna bağlı hemolitik anemi","synonyms":["Eritroenzimopatiye bağlı hemolitik anemi"]}},"xrefs":[{"source":"ICD-10","code":"D55.3","qualifier":"E","icd_relation":"specific","validated":true},{"source":"ICD-11","code":"3A10.Y","qualifier":"NTBT","icd_relation":"index","validated":true,"icd11_uri":"1788504817"},{"source":"UMLS","code":"C5680359","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"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":86817,"name":"Hemolytic anemia due to adenylate kinase deficiency","type":"Disease"},{"orpha":99138,"name":"Hemolytic anemia due to erythrocyte adenosine deaminase overproduction","type":"Disease"},{"orpha":35120,"name":"Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}