{"orpha":498445,"name":"Genetic inflammatory or rheumatoid-like osteoarthropathy","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-498445/","orphanet_url":"https://www.orpha.net/en/disease/detail/498445","names":{"fr":{"name":"Ostéoarthropathie génétique inflammatoire ou rhumatoïde-like"},"de":{"name":"Genetisch bedingte inflammatorische oder rheumatoide Osteoarthropathie"},"es":{"name":"Osteoartropatía genética inflamatoria o tipo reumatoide"},"it":{"name":"Osteoartropatie infiammatorie/simil-reumatoidi di origine genetica"},"nl":{"name":"Genetische inflammatoire of reumatoïdeachtige osteoartropathie"},"pt":{"name":"Osteoartropatias inflamatórias / tipo reumatóide genéticas"},"pl":{"name":"Genetyczna osteoartropatia zapalna lub podobna do reumatoidalnej"},"cs":{"name":"Geneticky podmíněné zánětlivé nebo revmatoidní osteoartropatie"},"uk":{"name":"Генетично обумовлена запальна або ревматоїдна остеоартропатія"},"zh":{"name":"遗传性炎症或类风湿性骨关节病"},"tr":{"name":"Genetik inflamatuar veya romatoid benzeri osteoartropati"}},"xrefs":[{"source":"UMLS","code":"C5681235","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93419,"name":"Rare bone disease"},"parents":[{"orpha":364526,"name":"Primary bone dysplasia","classifications":[147,156,199]}],"children":[{"orpha":1451,"name":"CINCA syndrome","type":"Disease"},{"orpha":53715,"name":"Familial tumoral calcinosis","type":"Disease"},{"orpha":498474,"name":"Hyaline fibromatosis syndrome","type":"Disease"},{"orpha":77297,"name":"Majeed syndrome","type":"Disease"},{"orpha":1159,"name":"Progressive pseudorheumatoid dysplasia","type":"Disease"},{"orpha":210115,"name":"Sterile multifocal osteomyelitis with periostitis and pustulosis","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}