| dbo:description
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- Krankheit (de)
- medical condition (en)
- медичний стан (uk)
- malattia neurodegenerativa (it)
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| dbo:differentialDiagnosis
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| dbo:diseasesDB
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| dbo:geneReviewsId
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| dbo:geneReviewsName
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- MAPT-Related Frontotemporal Dementia (en)
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| dbo:icd10
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| dbo:icd9
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| dbo:medicalCause
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| dbo:medicalDiagnosis
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| dbo:meshId
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| dbo:omim
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| dbo:symptom
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| dbo:thumbnail
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| dbo:wikiPageExternalLink
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| dbo:wikiPageWikiLink
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| dbp:caption
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- This condition is inherited in an autosomal dominant manner. (en)
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| dbp:causes
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- Mutations in the MAPT gene. (en)
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| dbp:diagnosis
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- Clinical criteria, molecular genetic analysis, and brain imaging. (en)
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| dbp:differential
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- Pick's disease, sporadic progressive supranuclear palsy, corticobasal degeneration, Parkinson-plus syndromes, dementia with Lewy bodies, Parkinson's disease, and multiple system atrophy. (en)
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| dbp:diseasesdb
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| dbp:frequency
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- Estimated to affect 1 in 1 million people in the Netherlands. (en)
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| dbp:genereviewsname
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- MAPT-Related Frontotemporal Dementia (en)
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| dbp:genereviewsnbk
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| dbp:icd
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- 331.190000 (xsd:double)
- (en)
- G31.8 (en)
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| dbp:meshid
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| dbp:omim
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| dbp:onset
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| dbp:scholia
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| dbp:snomedCt
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| dbp:symptoms
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- Loss of inhibition, inappropriate emotional responses, restlessness, neglect of personal hygiene, dementia, hallucinations, delusions, Parkinson's-like features, semantic paraphasias, and echolalia. (en)
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| dbp:synonyms
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- FTDP-17, Frontotemporal dementia with parkinsonism-17, Familial Pick's disease, Wilhelmsen-Lynch disease. (en)
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| dbp:treatment
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- Palliative and symptomatic interventions. (en)
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| dbp:wikiPageUsesTemplate
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| dct:subject
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| gold:hypernym
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| rdf:type
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| rdfs:label
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- Frontotemporal dementia and parkinsonism linked to chromosome 17 (en)
- Démence frontotemporale liée au chromosome 17 (fr)
- Demenza frontotemporale e parkinsonismo associata al cromosoma 17 (it)
- FTDP-17 (ja)
- Otępienie czołowo-skroniowe i parkinsonizm sprzężony z chromosomem 17 (pl)
- Фронтотемпоральная деменция и паркинсонизм 17 хромосомы (ru)
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| owl:sameAs
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| foaf:depiction
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