{"orpha":101972,"name":"Combined T and B cell immunodeficiency","type":"Clinical group","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"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-101972/","orphanet_url":"https://www.orpha.net/en/disease/detail/101972","names":{"fr":{"name":"Déficit immunitaire combiné T et B","synonyms":["Immunodéficience combinée T et B"]},"de":{"name":"T- und B-Zell-Immundefekt, kombinierter"},"es":{"name":"Inmunodeficiencia combinada de células B y T"},"it":{"name":"Immunodeficienza combinata da cellule T e B"},"nl":{"name":"Gecombineerde T- en B-cel-immuundeficiëntie"},"pt":{"name":"Imunodeficiência combinada de células B e T"},"pl":{"name":"Złożony Niedobór odporności komórek T i B"},"cs":{"name":"Kombinovaná T a B buněčná imunodeficience"},"uk":{"name":"Комбінований Т- і В-клітинний імунодефіцит"},"zh":{"name":"T细胞和B细胞联合免疫缺陷"},"tr":{"name":"Kombine T ve B hücre immün yetmezliği"}},"xrefs":[{"source":"ICD-10","code":"D81","qualifier":"E","icd_relation":"specific","validated":true},{"source":"ICD-11","code":"4A01.1","qualifier":"E","icd_relation":"specific","validated":true,"icd11_uri":"1616506198"},{"source":"MONDO","code":"15131","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681793","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98004,"name":"Rare immune disease"},"parents":[{"orpha":179006,"name":"Primary immunodeficiency due to a defect in adaptive immunity","classifications":[156,195]}],"children":[{"orpha":480549,"name":"Non-severe combined immunodeficiency","type":"Clinical group"},{"orpha":183660,"name":"Severe combined immunodeficiency","type":"Clinical group"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}