{"orpha":34526,"name":"OBSOLETE: Genetic primary hypomagnesemia","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 Rare renal tubular disease","url":"https://raremap.alftech.space/d/ORPHA-34526/","orphanet_url":"https://www.orpha.net/en/disease/detail/34526","names":{"fr":{"name":"OBSOLETE : Hypomagnésémie primaire d'origine génétique"},"de":{"name":"OBSOLET: Hypomagnesiämie, primäre, genetisch bedingte"},"es":{"name":"OBSOLETO: Hipomagnesemia primaria genética"},"it":{"name":"OBSOLETO: Ipomagnesemia ereditaria primitiva"},"nl":{"name":"OBSOLEET: Genetische primaire hypomagnesiëmie"},"pt":{"name":"OBSOLETO: Hipomagnesemia primária genética"},"pl":{"name":"NIEAKTUALNE: Genetycznie uwarunkowana pierwotna hipomagnezemia"},"cs":{"name":"NEAKTUÁLNÍ: Familiární primární hypomagnesémie"},"uk":{"name":"ЗАСТАРІЛО: Генетично обумовлена первинна гіпомагніємія"},"zh":{"name":"遗传性原发低镁血症"},"tr":{"name":"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}