{"orpha":98360,"name":"Constitutional anemia due to iron metabolism disorder","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-98360/","orphanet_url":"https://www.orpha.net/en/disease/detail/98360","names":{"fr":{"name":"Anémie constitutionnelle due à une anomalie du métabolisme du fer"},"de":{"name":"Konstitutionelle Anämie durch Störung des Eisenstoffwechsels"},"es":{"name":"Anemia constitucional por trastorno del metabolismo del hierro"},"it":{"name":"Anemia costituzionale da anomalie del metabolismo del ferro"},"nl":{"name":"Constitutionele anemie als gevolg van een ijzerstofwisselingsstoornis"},"pt":{"name":"Doença do metabolismo do ferro e da síntese do heme"},"pl":{"name":"Niedokrwistość konstytucjonalna z powodu zaburzenia metabolizmu żelaza"},"cs":{"name":"Konstituční anémie způsobená poruchou metabolismu železa"},"uk":{"name":"Конституційна анемія внаслідок порушення обміну заліза"},"zh":{"name":"铁代谢异常所致造血成分相关性贫血"},"tr":{"name":"Demir metabolizması bozukluğuna bağlı yapısal anemi"}},"xrefs":[{"source":"UMLS","code":"C5681718","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97992,"name":"Rare hematologic disease"},"parents":[{"orpha":248296,"name":"Constitutional deficiency anemia","classifications":[156,194]}],"children":[{"orpha":48818,"name":"Aceruloplasminemia","type":"Disease"},{"orpha":1195,"name":"Congenital atransferrinemia","type":"Disease"},{"orpha":209981,"name":"IRIDA syndrome","type":"Disease"},{"orpha":83642,"name":"Microcytic anemia with liver iron overload","type":"Disease"},{"orpha":300298,"name":"Severe congenital hypochromic anemia with ringed sideroblasts","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}