{"orpha":695164,"name":"Combined immunodeficiency with low B cells and hypogammaglobulinemia","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":["CID with low B cells and hypogammaglobulinemia"],"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-695164/","orphanet_url":"https://www.orpha.net/en/disease/detail/695164","names":{"fr":{"name":"Déficit immunitaire combiné avec faible nombre de cellules B et hypogammaglobulinémie","synonyms":["CID avec faible nombre de cellules B et hypogammaglobulinémie","DIC avec faible nombre de cellules B et hypogammaglobulinémie","Immunodéficience combinée avec faible nombre de cellules B et hypogammaglobulinémie"]},"de":{"name":"Kombinierter Immundefekt mit verminderter Anzahl an B-Zellen und Hypogammaglobulinämie","synonyms":["CID mit reduzierten B-Zell-Zahlen und Hypogammaglobulinämie"]},"es":{"name":"Inmunodeficiencia combinada con niveles bajos de linfocitos B e hipogammaglobulinemia","synonyms":["CID con niveles bajos de linfocitos B e hipogammaglobulinemia","IDC con niveles bajos de linfocitos B e hipogammaglobulinemia"]},"it":{"name":"Immunodeficienza combinata grave con livelli bassi di cellule B e ipogammaglobulinemia","synonyms":["CID con livelli bassi di cellule B e ipogammaglobulinemia","CID con numero ridotto di linfociti B"]},"nl":{"name":"Gecombineerde immuundeficiëntie met laag aantal B-cellen en hypogammaglobulinemie","synonyms":["CID met laag aantal B-cellen en hypogammaglobulinemie"]},"pt":{"name":"Combined immunodeficiency with low B cells"},"pl":{"name":"Combined immunodeficiency with low B cells and hypogammaglobulinemia","synonyms":["CID with low B cells and hypogammaglobulinemia"]},"cs":{"name":"Combined immunodeficiency with low B cells and hypogammaglobulinemia","synonyms":["CID with low B cells and hypogammaglobulinemia"]}},"xrefs":[],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98004,"name":"Rare immune disease"},"parents":[{"orpha":480549,"name":"Non-severe combined immunodeficiency","classifications":[156,195,233]}],"children":[{"orpha":217390,"name":"Combined immunodeficiency due to DOCK8 deficiency","type":"Disease"},{"orpha":700205,"name":"Combined immunodeficiency due to IKBKB gain-of-function mutation","type":"Disease"},{"orpha":504530,"name":"Combined immunodeficiency due to Moesin deficiency","type":"Disease"},{"orpha":314689,"name":"Combined immunodeficiency due to STK4 deficiency","type":"Disease"},{"orpha":695172,"name":"Combined immunodeficiency due to dimerization defective IKAROS mutation","type":"Disease"},{"orpha":726442,"name":"Combined immunodeficiency with hypo/agammaglobulinemia and opportunistic infections","type":"Disease"},{"orpha":477661,"name":"IL21-related infantile inflammatory bowel disease","type":"Disease"},{"orpha":447731,"name":"NIK deficiency","type":"Disease"},{"orpha":39041,"name":"Omenn syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}