{"orpha":156212,"name":"Hypoglossia/aglossia","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-156212/","orphanet_url":"https://www.orpha.net/en/disease/detail/156212","names":{"fr":{"name":"Hypoglossie/aglossie"},"de":{"name":"Hypoglossie/Aglossie"},"es":{"name":"Hipoglosia/aglosia"},"it":{"name":"Ipoglossia/aglossia"},"nl":{"name":"Hypoglossie/aglossie"},"pt":{"name":"Hipoglossia/aglossia"},"pl":{"name":"Niedorozwój/brak języka"},"cs":{"name":"Hypoglosie/aglosie"},"uk":{"name":"Гіпоглосія/аглосія"},"zh":{"name":"舌发育不全/无舌"},"tr":{"name":"Hipoglossi / aglossia"}},"xrefs":[{"source":"ICD-10","code":"Q38.3","qualifier":"E","icd_relation":"specific","validated":true},{"source":"MONDO","code":"15497","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680662","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":183583,"name":"Genetic head and neck malformation","classifications":[156]},{"orpha":155832,"name":"Rare head and neck malformation","classifications":[147]},{"orpha":68329,"name":"Rare maxillo-facial surgical disease","classifications":[209]}],"children":[{"orpha":141152,"name":"Isolated congenital hypoglossia/aglossia","type":"Morphological anomaly"},{"orpha":156215,"name":"Oromandibular-limb anomalies syndrome","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}