{"orpha":95501,"name":"OBSOLETE: Congenital central diabetes insipidus","type":"Category","group":"Group of disorders","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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.<br/><br/>Instead, consider using Central diabetes insipidus","url":"https://raremap.alftech.space/d/ORPHA-95501/","orphanet_url":"https://www.orpha.net/en/disease/detail/95501","names":{"fr":{"name":"OBSOLETE : Diabète insipide d'origine centrale congénital"},"de":{"name":"OBSOLET: Diabetes insipidus, kongenitaler zentraler"},"es":{"name":"OBSOLETO: Diabetes insípida central congénita"},"it":{"name":"OBSOLETO: Diabete insipido centrale congenito"},"nl":{"name":"OBSOLEET: Congenitale centrale diabetes insipidus"},"pt":{"name":"OBSOLETO: Diabetes insipidus central, congénito"},"pl":{"name":"NIEAKTUALNE: Wrodzona osrodkowa moczówka prosta"},"cs":{"name":"NEAKTUÁLNÍ: Vrozený centrální diabetes insipidus"},"uk":{"name":"ЗАСТАРІЛО: Вроджений центральний нецукровий діабет"},"zh":{"name":"弃用：先天性中枢性尿崩症"},"tr":{"name":"Eski adı: Doğumsal santral diyabet insipidus"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":178029,"name":"Arginine vasopressin deficiency"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}