{"orpha":211053,"name":"Specific language disorder","type":"Clinical group","group":"Group of disorders","status":"active","flags":[],"synonyms":["Dysphasia"],"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-211053/","orphanet_url":"https://www.orpha.net/en/disease/detail/211053","names":{"fr":{"name":"Dysphasie"},"de":{"name":"Spezifische Sprachentwicklungsstörung","synonyms":["Dysphasie"]},"es":{"name":"Trastorno específico del lenguaje","synonyms":["Disfasia"]},"it":{"name":"Disturbo specifico del linguaggio","synonyms":["Disfasia"]},"nl":{"name":"Specifieke taalstoornis","synonyms":["Dysfasie"]},"pt":{"name":"Dificuldade específica de linguagem"},"pl":{"name":"Specyficzne zaburzenia językowe","synonyms":["Dysfazja"]},"cs":{"name":"Specifická porucha řeči","synonyms":["Dysfázie"]},"uk":{"name":"Специфічні мовні розлади","synonyms":["Дисфазія"]},"zh":{"name":"特定语言障碍","synonyms":["语言障碍"]},"tr":{"name":"Spesifik dil bozukluğu","synonyms":["Disfazi"]}},"xrefs":[{"source":"MONDO","code":"0016226","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"16226","qualifier":"E","icd_relation":null,"validated":true},{"source":"MeSH","code":"D000080888","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0454651","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":211047,"name":"Specific learning disability","classifications":[181]}],"children":[{"orpha":251061,"name":"7q31 microdeletion syndrome","type":"Malformation syndrome"},{"orpha":1799,"name":"Familial developmental dysphasia","type":"Clinical syndrome"},{"orpha":436151,"name":"Intellectual disability-expressive aphasia-facial dysmorphism syndrome","type":"Malformation syndrome"},{"orpha":209908,"name":"Isolated childhood apraxia of speech","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}