{"orpha":619340,"name":"Inherited hematologic cancer-predisposing syndrome","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-619340/","orphanet_url":"https://www.orpha.net/en/disease/detail/619340","names":{"fr":{"name":"Syndrome héréditaire de prédisposition aux cancers hématologiques"},"de":{"name":"Krebsprädispositionssyndrom, hämatologisches hereditäres"},"es":{"name":"Síndrome de predisposición al cáncer hematológico hereditario"},"it":{"name":"Sindrome ereditaria da predisposizione ai tumori ematologici"},"nl":{"name":"Erfelijke hematologische kanker-predispositiesyndroom"},"pt":{"name":"Síndrome de predisposição a cancro hematológico hereditário"},"pl":{"name":"Wrodzony zespół predyspozycji do nowotworów układu krwiotwórczego"},"cs":{"name":"Dědičný syndromy predisponující k hematologické malignitě"},"uk":{"name":"Спадковий синдром схильності до раку крові"}},"xrefs":[{"source":"MONDO","code":"0850064","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681832","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":250908,"name":"Rare neoplastic disease"},"parents":[{"orpha":140162,"name":"Inherited cancer-predisposing syndrome","classifications":[156,202]}],"children":[{"orpha":697385,"name":"Combined immunodeficiency-cancer predisposing syndrome due to AIOLOS deficiency","type":"Disease"},{"orpha":488647,"name":"DDX41-related hematologic malignancy predisposition syndrome","type":"Disease"},{"orpha":697414,"name":"Early-onset combined immunodeficiency with low Ig due to dominant negative IKAROS mutation","type":"Disease"},{"orpha":71290,"name":"Familial platelet disorder with associated myeloid malignancy","type":"Disease"},{"orpha":319465,"name":"Inherited acute myeloid leukemia","type":"Disease"},{"orpha":524,"name":"Li-Fraumeni syndrome","type":"Disease"},{"orpha":648,"name":"Noonan syndrome","type":"Malformation syndrome"},{"orpha":500,"name":"Noonan syndrome with multiple lentigines","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}