{"orpha":696851,"name":"Common variable immunodeficiency and related disorders","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":["CVID and related disorders"],"definition":null,"note":"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.","url":"https://raremap.alftech.space/d/ORPHA-696851/","orphanet_url":"https://www.orpha.net/en/disease/detail/696851","names":{"fr":{"name":"Déficit immunitaire commun variable et maladies associées","synonyms":["CVID et maladies associées","DICV et maladies associées","Immunodéficience commune variable et maladies associées"]},"de":{"name":"Variables Immundefektsyndrom und verwandte Störungen","synonyms":["CVID und verwandte Krankheiten"]},"es":{"name":"Inmunodeficiencia común variable y trastornos relacionados","synonyms":["IDCV y trastornos relacionados"]},"it":{"name":"Immunodeficienza comune variabile e malattie correlate","synonyms":["CVID e malattie correlate"]},"nl":{"name":"Gewone variabele immuundeficiëntie en gerelateerde aandoeningen","synonyms":["CVID en gerelateerde aandoeningen"]},"pt":{"name":"Common variable immunodeficiency and related disorders"},"pl":{"name":"Common variable immunodeficiency and related disorders","synonyms":["CVID and related disorders"]},"cs":{"name":"Common variable immunodeficiency and related disorders","synonyms":["CVID and related disorders"]}},"xrefs":[],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":1572,"name":"OBSOLETE: Common variable immunodeficiency","status":"inactive"},{"type":"Referred to","orpha":77303,"name":"OBSOLETE: Common variable immunodeficiency due to an intrinsic B cell defect","status":"inactive"},{"type":"Referred to","orpha":99831,"name":"OBSOLETE: Common variable immunodeficiency due to an intrinsic T cell defect","status":"inactive"},{"type":"Referred to","orpha":183672,"name":"OBSOLETE: Common variable immunodeficiency due to TNFR deficiency","status":"inactive"},{"type":"Referred to","orpha":700746,"name":"OBSOLETE: Genetic common variable immunodeficiency phenotype and related disorders","status":"inactive"}],"preferential_parent":{"orpha":98004,"name":"Rare immune disease"},"parents":[{"orpha":101977,"name":"Immunodeficiency due to predominantly antibodies defect","classifications":[156,195]}],"children":[{"orpha":696857,"name":"Common variable immunodeficiency phenotype due to germinal digenic/polygenic mutations","type":"Disease"},{"orpha":696870,"name":"Common variable immunodeficiency phenotype due to germinal monogenic mutation","type":"Category"},{"orpha":696863,"name":"Common variable immunodeficiency phenotype due to somatic mutations","type":"Disease"},{"orpha":231205,"name":"Common variable immunodeficiency without known genetic defect","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":["Adolescent","Adult","Childhood"],"prevalence":[{"type":"Point prevalence","qualification":"Value and class","class":"1-9 / 100 000","value":2.5,"area":"Worldwide","status":"Validated","source":"ORPHANET"}],"phenotypes":null}