{"orpha":319612,"name":"OBSOLETE: X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency","type":"Etiological subtype","group":"Subtype of disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: X-linked MSMD due to IKBKG deficiency","OBSOLETE: X-linked MSMD due to NEMO deficiency","OBSOLETE: X-linked mendelian susceptibility to mycobacterial diseases due to NEMO deficiency"],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Hypohidrotic ectodermal dysplasia with immunodeficiency","url":"https://raremap.alftech.space/d/ORPHA-319612/","orphanet_url":"https://www.orpha.net/en/disease/detail/319612","names":{"fr":{"name":"OBSOLETE : Prédisposition mendélienne aux infections mycobactériennes liée à l'X par déficit en IKBKG","synonyms":["OBSOLETE : MSMD liée à l'X par déficit en IKBKG","OBSOLETE : MSMD liée à l'X par déficit en NEMO","OBSOLETE : Prédisposition mendélienne aux infections mycobactériennes liée à l'X par déficit en NEMO"]},"de":{"name":"OBSOLET: X-chromosomale Suszeptibilität für Mykobakteriosen durch IKBKG-Defekt"},"es":{"name":"OBSOLETO: Susceptibilidad mendeliana a enfermedades micobacterianas ligada al cromosoma X por deficiencia de IKBKG","synonyms":["OBSOLETO: SMEM ligada al cromosoma X por deficiencia de IKBKG","OBSOLETO: SMEM ligada al cromosoma X por deficiencia de NEMO","OBSOLETO: Susceptibilidad mendeliana a enfermedades micobacterianas ligada al cromosoma X por deficiencia de NEMO"]},"it":{"name":"OBSOLETO: Suscettibilit mendeliana a malattie micobatteriche, legata all'X , da deficit di IKBKG","synonyms":["OBSOLETO: MSMD legata all'X da deficit di IKBKG","OBSOLETO: MSMD legata all'X da deficit di NEMO","OBSOLETO: Suscettibilità mendeliana a malattie micobatteriche, legata all'X, da deficit di NEMO"]},"nl":{"name":"OBSOLEET: X-gebonden Mendeliaanse gevoeligheid voor mycobacteriële ziekten door IKBKG-deficiëntie","synonyms":["OBSOLEET: X-gebonden MSMD door IKBKG-deficiëntie","OBSOLEET: X-gebonden MSMD door NEMO-deficiëntie","OBSOLEET: X-gebonden Mendeliaanse gevoeligheid voor mycobacteriële ziekten door NEMO-deficiëntie"]},"pt":{"name":"OBSOLETO: Susceptibilidade mendeliana a doenças micobacterianas por deficiência de IKBKG ligada ao X"},"pl":{"name":"NIEAKTUALNE: Mendlowska podatność na choroby mykobakteryjne sprzężona z chromosomem X spowodowana niedoborem IKBKG","synonyms":["NIEAKTUALNE: Mendlowska podatność na choroby mykobakteryjne sprzężona z chromosomem X spowodowana niedoborem NEMO","NIEAKTUALNE: MSMD sprzężona z chromosomem X spowodowana niedoborem IKBKG","NIEAKTUALNE: MSMD sprzężona z chromosomem X spowodowana niedoborem NEMO"]},"cs":{"name":"NEAKTUÁLNÍ: X-vázaná genetická vnímavost k mykobakteriální infekci způsobená IKBKG deficitem","synonyms":["NEAKTUÁLNÍ: X-vázaná MSMD způsobená IKBKG deficitem","NEAKTUÁLNÍ: X-vázaná MSMD způsobená NEMO deficitem","NEAKTUÁLNÍ: X-vázaná genetická vnímavost k mykobakteriální infekci způsobená NEMO deficitem"]},"uk":{"name":"Х-зчеплена менделівська схильність до мікобактеріальних захворювань внаслідок дефіциту IKBKG","synonyms":["Х-зчеплена менделівська схильність до мікобактеріальних захворювань через дефіцит NEMO","Х-зчеплена MSMD внаслідок дефіциту IKBKG","Х-зчеплена MSMD через дефіцит NEMO"]},"zh":{"name":"IKBKG基因部分缺陷所致孟德尔X连锁遗传易感分枝杆菌病","synonyms":["IKBKG基因缺陷所致X连锁MSMD"]},"tr":{"name":"IKBKG eksikliğine bağlı mikobakteriyel hastalıklara X'e bağlı Mendel tipi yatkınlık","synonyms":["NEMO eksikliğine bağlı mikobakteriyel hastalıklara X'e bağlı Mendelian yatkınlık","NEMO eksikliğine bağlı X'e bağlı MSMD","IKBKG eksikliğine bağlı X'e bağlı MSMD"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":98813,"name":"Hypohidrotic ectodermal dysplasia with immunodeficiency"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}