{"orpha":279911,"name":"Primary organ-specific lymphoma","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-279911/","orphanet_url":"https://www.orpha.net/en/disease/detail/279911","names":{"fr":{"name":"Lymphome primaire spécifique d'organe"},"de":{"name":"Organ-spezifisches Lymphom, primäres"},"es":{"name":"Linfoma órgano-específico primario"},"it":{"name":"Linfoma organo-specifico primitivo"},"nl":{"name":"Primair orgaanspecifiek lymfoom"},"pt":{"name":"Linfoma órgão-específico primário"},"pl":{"name":"Pierwotny chłoniak specyficzny narządowo"},"cs":{"name":"Primární orgánově specifický lymfom"},"uk":{"name":"Первинна органоспецифічна лімфома"},"zh":{"name":"原发性器官特异性淋巴瘤"},"tr":{"name":"Primer organa özgü lenfoma"}},"xrefs":[{"source":"MONDO","code":"0017207","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"17207","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680788","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":250908,"name":"Rare neoplastic disease"},"parents":[{"orpha":223735,"name":"Lymphoma","classifications":[194,202,233]}],"children":[{"orpha":314684,"name":"Primary bone lymphoma","type":"Disease"},{"orpha":46135,"name":"Primary central nervous system lymphoma","type":"Disease"},{"orpha":714046,"name":"Primary choroidal lymphoma","type":"Disease"},{"orpha":542,"name":"Primary cutaneous lymphoma","type":"Category"},{"orpha":319667,"name":"Primary lymphoma of the conjunctiva","type":"Disease"},{"orpha":279897,"name":"Primary oculocerebral lymphoma","type":"Disease"},{"orpha":2420,"name":"Primary pulmonary lymphoma","type":"Disease"},{"orpha":97285,"name":"Thyroid lymphoma","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}