{"orpha":306522,"name":"OBSOLETE: Genetic primary hypomagnesemia with normocalciuria","type":"Clinical group","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 Rare renal tubular disease","url":"https://raremap.alftech.space/d/ORPHA-306522/","orphanet_url":"https://www.orpha.net/en/disease/detail/306522","names":{"fr":{"name":"OBSOLETE : Hypomagnésémie primaire d'origine génétique avec normocalciurie"},"de":{"name":"OBSOLET: Hypomagnesiämie mit Normokalziurie, genetisch bedingte"},"es":{"name":"OBSOLETO: Hipomagnesemia primaria genética con normocalciuria"},"it":{"name":"OBSOLETO: ipomagnesemia primitiva genetica normocalciurica"},"nl":{"name":"OBSOLEET: Genetische primaire hypomagnesiëmie met normocalciurie"},"pt":{"name":"OBSOLETO: Hipomagnesemia primária genética com normocalciúria"},"pl":{"name":"NIEAKTUALNE: Genetycznie uwarunkowana pierwotna hipomagnezemia z normokalciurią"},"cs":{"name":"NEAKTUÁLNÍ: Familiární primární hypomagnezémie s normokalciurií"},"uk":{"name":"ЗАСТАРІЛО: Генетично обумовлена первинна гіпомагніємія з нормокальціурією"},"zh":{"name":"遗传性原发性低镁血症伴正常钙尿","definition":"家族性原发性低镁血症伴尿钙正常 （FPHN）是一种家族性原发性低镁血症（FPH；见本术语），其特征是血清镁降低，血钙正常。该病有三种类型：常染色体隐性遗传原发性低镁血症伴尿钙正常和低血钙（ARPHN）、家族性原发性低镁血症伴尿钙血钙正常（FPHNN）和Glaudemans型孤立性常染色体显性遗传低镁血症（见这些术语）。"},"tr":{"name":"Normokalsiüri ile seyreden genetik primer hipomagnezemi"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":93603,"name":"Rare renal tubular disease"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}