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| Term | frontotemporal dementia | ID (Ontology) | DOID:9255 (Human Disease) | |||||||||||||||||||||||||||||||||||
| Definition | A dementia characterized by progressive neuronal loss predominantly involving the frontal and/or temporal lobes of the brain resulting in a gradual and progressive decline in behavior or language. | |||||||||||||||||||||||||||||||||||||
| Also Known As | "frontotemporal lobar degeneration" ; "multiple system tauopathy with presenile dementia" ; "pallidopontonigral degeneration" (for all, see Synonyms field below) | |||||||||||||||||||||||||||||||||||||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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cognitive disorder |__dementia____________________ central nervous system disease | |__brain disease_______________| frontotemporal dementia 180 rec. |__corticobasal degeneration syndrome |__frontotemporal dementia and/or amyotrophic lateral sclerosis 7 41 rec. |__GRN-related frontotemporal lobar degeneration with Tdp43 inclusions |__Pick's disease 6 rec. |__primary progressive aphasia |__logopenic progressive aphasia |__progressive non-fluent aphasia |__semantic dementia |
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| Is a |
dementia brain disease |
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Synonyms & Secondary IDs
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External Crossreferences & Linkouts
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GARD:8436 MESH:C563003 MIM:600274 ORDO:282 SNOMEDCT_US_2023_03_01:42369001 UMLS_CUI:C0520716 |
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