{"orpha":696863,"name":"Common variable immunodeficiency phenotype due to somatic mutations","type":"Disease","group":"Disorder","status":"active","flags":[],"synonyms":["CVID phenotype due to somatic mutations"],"definition":null,"note":null,"url":"https://raremap.alftech.space/d/ORPHA-696863/","orphanet_url":"https://www.orpha.net/en/disease/detail/696863","names":{"fr":{"name":"Phénotype de déficit immunitaire commun variable associé à des mutations somatiques","synonyms":["Phénotype d'immunodéficience commune variable associé à des mutations somatiques","Phénotype de CVID associé à des mutations somatiques","Phénotype de DICV associé à des mutations somatiques"]},"de":{"name":"Variables Immundefekt-Syndrom durch somatische Mutationen","synonyms":["CVID durch somatische Mutationen"]},"es":{"name":"Fenotipo de inmunodeficiencia común variable por mutaciones somáticas","synonyms":["Fenotipo de IDCV por mutaciones somáticas"]},"it":{"name":"Fenotipo dell’immunodeficienza comune variabile da mutazioni somatiche","synonyms":["Fenotipo della CVID da mutazioni somatiche"]},"nl":{"name":"Fenotype van gewone variabele immuundeficiëntie door somatische mutaties","synonyms":["CVID-fenotype door somatische mutaties"]},"pt":{"name":"Common variable immune deficiency phenotype due to somatic mutations"},"pl":{"name":"Common variable immunodeficiency phenotype due to somatic mutations","synonyms":["CVID phenotype due to somatic mutations"]},"cs":{"name":"Common variable immunodeficiency phenotype due to somatic mutations","synonyms":["CVID phenotype due to somatic 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":["Not applicable"],"onset":["Adolescent","Adult","Childhood"],"prevalence":[{"type":"Point prevalence","qualification":"Class only","class":"Unknown","value":0.0,"area":"Worldwide","status":"Validated","source":"ORPHANET"}],"phenotypes":null}