{"orpha":183710,"name":"Genetic susceptibility to infections due to particular pathogens","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-183710/","orphanet_url":"https://www.orpha.net/en/disease/detail/183710","names":{"fr":{"name":"Prédisposition génétique aux infections à pathogènes particuliers"},"de":{"name":"Genetische Prädisposition für Infektionen durch spezifische Pathogene"},"es":{"name":"Susceptibilidad genética a infecciones por patógenos particulares"},"it":{"name":"Suscettibilità genetica da infezioni dovute a patogeni particolari"},"nl":{"name":"Genetische gevoeligheid voor infecties door specifieke pathogenen"},"pt":{"name":"Predisposição para infeções bacterianas invasivas"},"pl":{"name":"Genetyczna podatność na infekcje wywoływane przez szczególne patogeny"},"cs":{"name":"Geneticky podmíněná náchylnost k infekcím specifickými patogeny"},"uk":{"name":"Генетично обумовлена схильність до інфекцій, спричинених певними патогенами"},"zh":{"name":"特定病原体感染的遗传易感性"},"tr":{"name":"Belirli patojenlere bağlı enfeksiyonlara genetik yatkınlık"}},"xrefs":[{"source":"ICD-11","code":"4A00.2","qualifier":"E","icd_relation":"specific","validated":true,"icd11_uri":"1946750030"},{"source":"MONDO","code":"15979","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680530","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98004,"name":"Rare immune disease"},"parents":[{"orpha":101988,"name":"Primary immunodeficiency due to a defect in innate immunity","classifications":[156,195]}],"children":[{"orpha":1334,"name":"Chronic mucocutaneous candidiasis","type":"Disease"},{"orpha":726479,"name":"Genetic predisposition to Whipple disease due to IRF4 haploinsufficiency","type":"Disease"},{"orpha":1930,"name":"Herpes simplex virus encephalitis","type":"Disease"},{"orpha":302,"name":"Inherited epidermodysplasia verruciformis","type":"Disease"},{"orpha":748,"name":"Mendelian susceptibility to mycobacterial diseases","type":"Clinical group"},{"orpha":457088,"name":"Predisposition to invasive fungal disease due to CARD9 deficiency","type":"Disease"},{"orpha":391487,"name":"STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome","type":"Disease"},{"orpha":391311,"name":"Susceptibility to viral and mycobacterial infections due to STAT1 deficiency","type":"Disease"},{"orpha":324294,"name":"T-cell immunodeficiency with epidermodysplasia verruciformis","type":"Disease"},{"orpha":70592,"name":"Transient predisposition to invasive pyogenic bacterial infection","type":"Disease"},{"orpha":51636,"name":"WHIM syndrome","type":"Disease"},{"orpha":3452,"name":"Whipple disease","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}