{"orpha":183770,"name":"Rare genetic immune disease","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-183770/","orphanet_url":"https://www.orpha.net/en/disease/detail/183770","names":{"fr":{"name":"Maladie immunologique rare d'origine génétique"},"de":{"name":"Immunkrankheit, genetisch bedingte, seltene"},"es":{"name":"Enfermedades inmunológicas genéticas raras"},"it":{"name":"Malattia genetica autoimmune rara"},"nl":{"name":"Zeldzame genetische immuunziekte"},"pt":{"name":"Doença imune genética rara"},"pl":{"name":"Rzadka choroba immunologiczna uwarunkowana genetycznie"},"cs":{"name":"Vzácné dědičné poruchy imunitního systému"},"uk":{"name":"Рідкісне генетично обумовлене імунне захворювання"},"zh":{"name":"罕见遗传性免疫疾病"},"tr":{"name":"Nadir genetik bağışıklık hastalığı"}},"xrefs":[{"source":"MONDO","code":"15984","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680526","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98004,"name":"Rare immune disease"},"parents":[{"orpha":98053,"name":"Rare genetic disease","classifications":[156]}],"children":[{"orpha":91378,"name":"Hereditary angioedema","type":"Clinical group"},{"orpha":279943,"name":"Hereditary neutrophilia","type":"Disease"},{"orpha":728475,"name":"Inherited bone marrow failure disorder with immune defect","type":"Category"},{"orpha":101997,"name":"Primary immunodeficiency","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}