{"orpha":331244,"name":"OBSOLETE: Other immunodeficiency syndrome with predominantly antibody defects","type":"Category","group":"Group of disorders","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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.<br/><br/>Instead, consider using Immunodeficiency predominantly affecting antibody production","url":"https://raremap.alftech.space/d/ORPHA-331244/","orphanet_url":"https://www.orpha.net/en/disease/detail/331244","names":{"fr":{"name":"OBSOLETE : Autre syndrome de déficit immunitaire par déficit de production d'anticorps","synonyms":["OBSOLETE : Autre syndrome d'immunodéficience par déficit de production d'anticorps"]},"de":{"name":"OBSOLET: Sonstiges Immundefekt-Syndrom mit vorwiegendem Antikörper-Defekt"},"es":{"name":"OBSOLETO: Otros síndromes de inmunodeficiencia con defectos predominantes de anticuerpos"},"it":{"name":"OBSOLETO: Altra sindrome da immunodeficienza con difetti predominanti degli anticorpi"},"nl":{"name":"OBSOLEET: Ander immuundeficiëntiesyndroom met predominante antilichaamdefecten"},"pt":{"name":"OBSOLETO: Outra síndrome de imunodeficiência com predominância defeitos de anticorpos"},"pl":{"name":"NIEAKTUALNE: Inny zespół z niedoborem odporności z dominującymi defektami przeciwciał"},"cs":{"name":"NEAKTUÁLNÍ: Jiný syndrom imunodeficience s převažující poruchou protilátek"},"uk":{"name":"Інші синдроми імунодефіциту з переважним дефіцитом антитіл"},"zh":{"name":"以抗体缺陷为主的其他免疫缺陷综合征"},"tr":{"name":"Ağırlıklı antikor defekti ile seyreden diğer immün yetmezlik sendromu"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":101977,"name":"Immunodeficiency due to predominantly antibodies defect"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}