{"orpha":98396,"name":"Constitutional megaloblastic anemia due to vitamin B12 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-98396/","orphanet_url":"https://www.orpha.net/en/disease/detail/98396","names":{"fr":{"name":"Anémie mégaloblastique constitutionnelle due à une anomalie de métabolisme de la vitamine B12"},"de":{"name":"Anämie, megaloblastische, Vitamin B12-abhängig"},"es":{"name":"Anemia megaloblástica constitucional por trastorno del metabolismo de la vitamina B12"},"it":{"name":"Anemia megaloblastica costituzionale da disturbi del metabolismo della vitamina B12"},"nl":{"name":"Constitutionele megaloblastische anemie als gevolg van vitamine B12-stofwisselingsstoornis"},"pt":{"name":"Anemia megaloblástica, relacionada com a vitamina B12"},"pl":{"name":"Niedokrwistość megaloblastyczna konstytucjonalna z powodu zaburzenia metabolizmu witaminy B12"},"cs":{"name":"Konstituční megaloblastická anémie způsobená poruchou metabolismu vitaminu B12"},"uk":{"name":"Конституціональна мегалобластна анемія внаслідок порушення обміну вітаміну В12"},"zh":{"name":"维生素B12代谢紊乱所致原发性巨幼细胞贫血"},"tr":{"name":"B12 vitamini metabolizması bozukluğuna bağlı yapısal megaloblastik anemi"}},"xrefs":[{"source":"UMLS","code":"C5681709","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":332,"name":"Congenital intrinsic factor deficiency","type":"Disease"},{"orpha":622,"name":"Homocystinuria without methylmalonic aciduria","type":"Disease"},{"orpha":35858,"name":"Imerslund-Gräsbeck syndrome","type":"Disease"},{"orpha":26,"name":"Methylmalonic acidemia with homocystinuria","type":"Disease"},{"orpha":859,"name":"Transcobalamin II deficiency","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}