{"orpha":229720,"name":"Syndromic agammaglobulinemia","type":"Category","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-229720/","orphanet_url":"https://www.orpha.net/en/disease/detail/229720","names":{"fr":{"name":"Agammaglobulinémie syndromique"},"de":{"name":"Agammaglobulinämie, syndromale"},"es":{"name":"Agammaglobulinemia sindrómica"},"it":{"name":"Agammaglobulinemia sindromica"},"nl":{"name":"Syndromale agammaglobulinemie"},"pt":{"name":"Agamaglobulinemia sindromática"},"pl":{"name":"Agammaglobulinemia syndromiczna"},"cs":{"name":"Syndromická agamaglobulinémie"},"uk":{"name":"Синдромна агаммаглобулінемія"},"zh":{"name":"综合征性无丙种球蛋白血症"},"tr":{"name":"Sendromik agamaglobulinemi"}},"xrefs":[{"source":"MONDO","code":"0016463","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"16463","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680904","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98004,"name":"Rare immune disease"},"parents":[{"orpha":183669,"name":"Agammaglobulinemia","classifications":[156,195]}],"children":[{"orpha":693647,"name":"Agammaglobulinemia-early-onset hypertrophic cardiomyopathy-neutropenia syndrome","type":"Disease"},{"orpha":83617,"name":"Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome","type":"Malformation syndrome"},{"orpha":693627,"name":"Agammaglobulinemia-skin involvement-failure to thrive syndrome","type":"Disease"},{"orpha":567502,"name":"B-cell immunodeficiency-limb anomaly-urogenital malformation syndrome","type":"Disease"},{"orpha":632,"name":"Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia","type":"Clinical subtype"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}