{"orpha":100039,"name":"Familial pseudohyperkalemia type 1","type":"Clinical subtype","group":"Subtype of disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":[],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Dehydrated hereditary stomatocytosis","url":"https://raremap.alftech.space/d/ORPHA-100039/","orphanet_url":"https://www.orpha.net/en/disease/detail/100039","names":{"fr":{"name":"Pseudohyperkaliémie familiale type 1"},"de":{"name":"Pseudohyperkaliämie, familiäre, Typ 1"},"es":{"name":"Pseudohiperpotasemia familiar tipo 1"},"it":{"name":"Pseudoiperkaliemia familiare, tipo 1"},"nl":{"name":"Familiale pseudohyperkaliëmie type 1"},"pt":{"name":"Pseudohipercalemia, familiar, tipo 1"},"pl":{"name":"Rodzinna hiperkaliemia rzekoma typu 1"},"cs":{"name":"Familiární pseudohyperkalémie, typ 1"},"uk":{"name":"Сімейна псевдогіперкаліємія, тип 1"},"zh":{"name":"家族性假高血钾症1型"},"tr":{"name":"ailesel psödohiperkalemi tip 1"}},"xrefs":[],"associations":[{"type":"Moved to","orpha":3202,"name":"Dehydrated hereditary stomatocytosis"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}