{"orpha":1678,"name":"Dincsoy-Salih-Patel syndrome","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":["Facial dysmorphism-ambiguous genitalia-hypopituitarism-short limbs syndrome"],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Septo-optic dysplasia spectrum","url":"https://raremap.alftech.space/d/ORPHA-1678/","orphanet_url":"https://www.orpha.net/en/disease/detail/1678","names":{"fr":{"name":"Syndrome de Dincsoy-Salih-Patel","synonyms":["Syndrome de dysmorphie-ambiguïté génitale-hypopituitarisme-membres courts"]},"de":{"name":"Dincsoy-Salih-Patel-Syndrom","synonyms":["Faziale Dysmorphien - intersexuelles Genitale - Hypopituitarismus - kurze Extremitäten"]},"es":{"name":"Síndrome de Dincsoy-Salih-Patel"},"it":{"name":"Sindrome di Dincsoy-Salih-Patel","synonyms":["Dismorfismi facciali - genitali ambigui - ipopituitarismo - arti corti"]},"nl":{"name":"Syndroom van Dincsoy-Salih-Patel","synonyms":["Faciale dysmorfie - ambigue genitaliën - hypopituïtarisme - korte ledematen-syndroom"]},"pt":{"name":"Síndrome Dincsoy-Salih-Patel","synonyms":["Dismorfia facial-ambiguidade dos genitais-hipopituitarismo-membros curtos"]},"pl":{"name":"Zespół Dincsoy'a, Saliha i Patela","synonyms":["Dysmorfia twarzy - obojnacze narządy płciowe - hipopituitaryzm - krótkie kończyny"]},"cs":{"name":"Dincsoyův-Salihův-Patelův syndrom","synonyms":["Syndrom zahrnující faciální dysmorfismus, obojetný genitál, hypopituitarismus a krátké končetiny","Dincsoy-Salih-Patelův syndrom"]},"uk":{"name":"Синдром Дінчоя-Саліха-Пателя","synonyms":["Синдром дисморфізму обличчя - неоднозначних геніталій - гіпопітуїтаризма - коротких кінцівок"]},"zh":{"name":"Dincsoy-Salih-Patel综合征","synonyms":["面部畸形-两性畸形-垂体功能低下-短肢综合征"]},"tr":{"name":"Dincsoy-Salih-Patel sendromu","synonyms":["Fasiyal dismorfizmi-belirsiz cinsel organ-hipopituitarizm-kısa ekstremiteler sendromu"]}},"xrefs":[{"source":"OMIM","code":"601016","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C1832874","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":3157,"name":"Septo-optic dysplasia spectrum"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}