{"orpha":567562,"name":"Disorder with multisystemic involvement and glomerulopathy","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-567562/","orphanet_url":"https://www.orpha.net/en/disease/detail/567562","names":{"fr":{"name":"Maladie avec atteinte multisystémique et glomérulopathie"},"de":{"name":"Multisystemische Störung mit Glomerulopathie als Hauptmerkmal"},"es":{"name":"Trastorno con afectación multisistémico y glomerulopatía"},"it":{"name":"Malattia multisistemica con glomerulopatia"},"nl":{"name":"Aandoening met multisystemische betrokkenheid en glomerulopathie"},"pt":{"name":"Doença com envolvimento multissistémico e glomerulopatia"},"pl":{"name":"Zaburzenie z zajęciem wielu układów i glomerulopatią"},"cs":{"name":"Porucha s multisystémovým postižením a glomerulopatií"},"uk":{"name":"Захворювання з мультисистемним ураженням та гломерулопатією"},"zh":{"name":"多系统受累伴肾小球病变"},"tr":{"name":"Multisistemik tutulum ve glomerülopati ile seyreden bozukluk"}},"xrefs":[{"source":"UMLS","code":"C5681301","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93626,"name":"Rare renal disease"},"parents":[{"orpha":183586,"name":"Genetic glomerular disease","classifications":[156]},{"orpha":93548,"name":"Glomerular disease","classifications":[188,233]}],"children":[{"orpha":163696,"name":"Action myoclonus-renal failure syndrome","type":"Disease"},{"orpha":93114,"name":"Autosomal dominant intermediate Charcot-Marie-Tooth disease type E","type":"Disease"},{"orpha":69063,"name":"Congenital membranous nephropathy due to fetomaternal anti-neutral endopeptidase alloimmunization","type":"Disease"},{"orpha":220,"name":"Denys-Drash syndrome","type":"Disease"},{"orpha":506334,"name":"Familial steroid-resistant nephrotic syndrome with adrenal insufficiency","type":"Disease"},{"orpha":280406,"name":"Familial steroid-resistant nephrotic syndrome with sensorineural deafness","type":"Disease"},{"orpha":347,"name":"Frasier syndrome","type":"Disease"},{"orpha":2065,"name":"Galloway-Mowat syndrome","type":"Malformation syndrome"},{"orpha":69735,"name":"Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome","type":"Disease"},{"orpha":306504,"name":"Interstitial lung disease-nephrotic syndrome-epidermolysis bullosa syndrome","type":"Disease"},{"orpha":182050,"name":"MYH9-related syndromic thrombocytopenia","type":"Disease"},{"orpha":2614,"name":"Nail-patella syndrome","type":"Malformation syndrome"},{"orpha":2613,"name":"Nail-patella-like renal disease","type":"Disease"},{"orpha":300333,"name":"Nephrotic syndrome-epidermolysis bullosa-sensorineural deafness syndrome","type":"Disease"},{"orpha":2670,"name":"Pierson syndrome","type":"Malformation syndrome"},{"orpha":1830,"name":"Schimke immuno-osseous dysplasia","type":"Disease"},{"orpha":2715,"name":"Severe oculo-renal-cerebellar syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}