{"orpha":481671,"name":"Type 1 interferonopathy of childhood","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-481671/","orphanet_url":"https://www.orpha.net/en/disease/detail/481671","names":{"fr":{"name":"Interféronopathie type 1 de l'enfant"},"de":{"name":"Typ-1-Interferonopathie des Kindesalters"},"es":{"name":"Interferonopatía tipo 1 de la infancia"},"it":{"name":"Interferonopatia tipo 1 dell'infanzia"},"nl":{"name":"Type 1 interferonopathie van de kindertijd"},"pt":{"name":"Interferonopatia tipo 1 da infância"},"pl":{"name":"Interferonopatia dziecięca typu 1"},"cs":{"name":"Interferonopatie dětského věku, typ1"},"uk":{"name":"Дитяча інтерферонопатія, тип 1"},"zh":{"name":"儿童1型干扰素病"},"tr":{"name":"Tip 1 çocukluk çağı interferonopati"}},"xrefs":[{"source":"MONDO","code":"0957408","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681250","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98023,"name":"Rare systemic or rheumatologic disease"},"parents":[{"orpha":319719,"name":"Autoinflammatory syndrome of childhood","classifications":[231]}],"children":[{"orpha":51,"name":"Aicardi-Goutières syndrome","type":"Disease"},{"orpha":300345,"name":"Autosomal systemic lupus erythematosus","type":"Disease"},{"orpha":404553,"name":"Deficiency of adenosine deaminase 2","type":"Disease"},{"orpha":481662,"name":"Familial Chilblain lupus","type":"Disease"},{"orpha":319563,"name":"Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency","type":"Disease"},{"orpha":699605,"name":"NEMO deleted exon 5 autoinflammatory syndrome","type":"Disease"},{"orpha":324977,"name":"Proteasome-associated autoinflammatory syndrome","type":"Disease"},{"orpha":481665,"name":"Pseudo-TORCH syndrome type 2","type":"Disease"},{"orpha":714429,"name":"Pseudo-TORCH syndrome type 3","type":"Disease"},{"orpha":619367,"name":"SAMD9L-associated autoinflammatory syndrome","type":"Disease"},{"orpha":425120,"name":"STING-associated vasculopathy with onset in infancy","type":"Disease"},{"orpha":85191,"name":"Singleton-Merten dysplasia","type":"Malformation syndrome"},{"orpha":1855,"name":"Spondyloenchondrodysplasia","type":"Malformation syndrome"},{"orpha":84064,"name":"Trichohepatoenteric syndrome","type":"Disease"},{"orpha":85453,"name":"X-linked reticulate pigmentary disorder","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}