{"orpha":659387,"name":"PRC-2 complex-related overgrowth spectrum","type":"Clinical group","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-659387/","orphanet_url":"https://www.orpha.net/en/disease/detail/659387","names":{"fr":{"name":"Syndrome d'hypercroissance liée à complexe PRC-2"},"de":{"name":"PRC2-assoziiertes Überwuchsspektrum","synonyms":["PRC2-assoziiertes Großwuchssyndrom"]},"es":{"name":"Espectro de síndromes de sobrecrecimiento asociado al complejo PRC-2"},"it":{"name":"Spettro dell’iperaccrescimento correlato al complesso PRC-2"},"nl":{"name":"PRC-2-complex-gerelateerd overgroeispectrum"},"pt":{"name":"Espetro clínico de sobrecrescimento PRC-2 complexo-relacionado"},"pl":{"name":"Spektrum przerostu związanego z kompleksem PRC-2"},"cs":{"name":"Spektrum nadměrného vzrůstu související s komplexem PRC-2"},"uk":{"name":"Спектр надмірного росту, повязаний з комплексом PRC-2"}},"xrefs":[{"source":"UMLS","code":"C5925135","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[{"type":"Moved to","orpha":3446,"name":"Weaver-like syndrome","status":"inactive"}],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":611327,"name":"Genetic multiple congenital anomalies/dysmorphic syndrome-intellectual disability","classifications":[156]},{"orpha":102283,"name":"Multiple congenital anomalies/dysmorphic syndrome-intellectual disability","classifications":[147,181]},{"orpha":498448,"name":"Overgrowth or tall stature syndrome with skeletal involvement","classifications":[147,156,199]},{"orpha":93460,"name":"Overgrowth syndrome","classifications":[147,156]}],"children":[{"orpha":659396,"name":"Cohen-Gibson syndrome","type":"Malformation syndrome"},{"orpha":659463,"name":"Imagawa-Matsumoto syndrome","type":"Malformation syndrome"},{"orpha":3447,"name":"Weaver syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}