{"orpha":1572,"name":"OBSOLETE: Common variable immunodeficiency","type":"Disease","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: CVID"],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Common variable immunodeficiency and related disorders","url":"https://raremap.alftech.space/d/ORPHA-1572/","orphanet_url":"https://www.orpha.net/en/disease/detail/1572","names":{"fr":{"name":"OBSOLETE : Déficit immunitaire commun variable","synonyms":["OBSOLETE : CVID","OBSOLETE : DICV","OBSOLETE : Immunodéficience commune variable"]},"de":{"name":"OBSOLET: Immundefektsyndrom, variables","synonyms":["OBSOLET: CVID"]},"es":{"name":"OBSOLETO: Inmunodeficiencia común variable","synonyms":["OBSOLETO: IDCV"]},"it":{"name":"OBSOLETO: Immunodeficienza variabile comune","synonyms":["OBSOLETO: Deficit idiopatico di immunoglobuline","OBSOLETO: Deficit primitivo di anticorpi","OBSOLETO: Ipogammaglobulinemia primitiva"]},"nl":{"name":"OBSOLEET: Gewone variabele immuundeficiëntie","synonyms":["OBSOLEET: CVID","OBSOLEET: Idiopathische deficiëntie van immunoglobuline","OBSOLEET: Primaire deficiëntie van antilichamen","OBSOLEET: Primaire hypogammaglobulinemie"]},"pt":{"name":"OBSOLETO: Imunodeficiência variável comum"},"pl":{"name":"NIEAKTUALNE: Pospolity zmienny Niedobór odporności","synonyms":["NIEAKTUALNE: CVID","NIEAKTUALNE: Idiopatyczny Niedobór immunoglobulin","NIEAKTUALNE: Pierwotna hipogammaglobulinemia","NIEAKTUALNE: Pierwotny Niedobór przeciwciał"]},"cs":{"name":"NEAKTUÁLNÍ: Běžná variabilní imunodeficience","synonyms":["NEAKTUÁLNÍ: CVID","NEAKTUÁLNÍ: Primární protilátková imunodeficience","NEAKTUÁLNÍ: Primární hypogamaglobulinemie","NEAKTUÁLNÍ: Idiopatický deficit imunoglobulinů"]},"uk":{"name":"Загальний варіабельний імунодефіцит","synonyms":["CVID","Ідіопатичний дефіцит імуноглобулінів","Первинний дефіцит антитіл","Первинна гіпогаммаглобулінемія"],"definition":"Common variable immunodeficiency (CVID) comprises a heterogeneous group of diseases characterized by a significant hypogammaglobulinemia of unknown cause, failure to produce specific antibodies after immunizations and susceptibility to bacterial infections, predominantly caused by encapsulated bacteria."},"zh":{"name":"普通变异型免疫缺陷病","synonyms":["特发性免疫球蛋白缺乏症"]},"tr":{"name":"Yaygın değişken immün yetmezlik","synonyms":["CVID","Primer antikor eksikliği","Primer hipogammaglobulinemi","İdiyopatik immünoglobulin eksikliği"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":696851,"name":"Common variable immunodeficiency and related disorders"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}