{"orpha":696857,"name":"Common variable immunodeficiency phenotype due to germinal digenic/polygenic mutations","type":"Disease","group":"Disorder","status":"active","flags":[],"synonyms":["CVID phenotype due to germinal digenic/polygenic mutations"],"definition":null,"note":null,"url":"https://raremap.alftech.space/d/ORPHA-696857/","orphanet_url":"https://www.orpha.net/en/disease/detail/696857","names":{"fr":{"name":"Phénotype de déficit immunitaire commun variable associé à des mutations germinales digéniques/polygéniques","synonyms":["Phénotype d'immunodéficience commune variable associé à des mutations germinales digéniques/polygéniques","Phénotype de CVID associé à des mutations germinales digéniques/polygéniques","Phénotype de DICV associé à des mutations germinales digéniques/polygéniques"]},"de":{"name":"Variables Immundefekt-Syndrom durch digene/polygene Keimbahnmutationen","synonyms":["CVID durch digene/polygene Mutationen der Keimbahn"]},"es":{"name":"Fenotipo de inmunodeficiencia común variable por mutaciones digénicas/poligénicas germinales","synonyms":["Fenotipo de IDCV por mutaciones digénicas/poligénicas germinales"]},"it":{"name":"Fenotipo dell’immunodeficienza comune variabile da mutazioni germinali digeniche/poligeniche","synonyms":["Fenotipo della CVID da mutazioni germinali digeniche/poligeniche"]},"nl":{"name":"Fenotype van gewone variabele immuundeficiëntie door digene/polygene kiembaanmutaties","synonyms":["CVID-fenotype door digene/polygene kiembaanmutaties"]},"pt":{"name":"Common variable immunodeficiency phenotype due to germinal digenic/polygenic mutations"},"pl":{"name":"Common variable immunodeficiency phenotype due to germinal digenic/polygenic mutations","synonyms":["CVID phenotype due to germinal digenic/polygenic mutations"]},"cs":{"name":"Common variable immunodeficiency phenotype due to germinal digenic/polygenic mutations","synonyms":["CVID phenotype due to germinal digenic/polygenic mutations"]}},"xrefs":[],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98004,"name":"Rare immune disease"},"parents":[{"orpha":696851,"name":"Common variable immunodeficiency and related disorders","classifications":[156,195]}],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":["Multigenic/multifactorial"],"onset":["Adolescent","Adult","Childhood"],"prevalence":[{"type":"Point prevalence","qualification":"Class only","class":"Unknown","value":0.0,"area":"Worldwide","status":"Validated","source":"ORPHANET"}],"phenotypes":null}