Frontotemporal dementia (FTD) comprises a group of neurodegenerative disorders, characterized by progressive changes in behavior, executive dysfunction and language impairment, as a result of degeneration of the medial prefrontal and frontoinsular cortices. Four clinical subtypes have been identified: semantic dementia, progressive non-fluent aphasia, behavioral variant FTD and right temporal lobar atrophy (see these terms).
Synonyms: FTD
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Term information
database cross reference
- ICD-10:G31.0 (Attributed (The ICD10 code is attributed by Orphanet))
- MedDRA:10068968 (E (Exact mapping: the two concepts are equivalent))
- OMIM:607485 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
- MeSH:D057180 (E (Exact mapping: the two concepts are equivalent))
- OMIM:600795 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
- ICD-10:G31.0 (NTBT (ORPHA code's Narrower Term maps to a Broader Term))
- UMLS:C0338451 (E (Exact mapping: the two concepts are equivalent))
- OMIM:172700 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
- OMIM:600274 (E (Exact mapping: the two concepts are equivalent))
hasDbXref
OMIM:600274
ICD-10:G31.0
OMIM:600795
OMIM:607485
MedDRA:10068968
OMIM:172700
MeSH:D057180
UMLS:C0338451
Term relations
Subclass of:
- Genetic frontotemporal degeneration with dementia
- Frontotemporal degeneration with dementia
- has_annual_incidence_range some 1-9 / 100 000 and present_in some Italy and has_annual_incidence_average_value value 3.05
- has_inheritance some autosomal dominant
- has_age_of_onset some adult
- present_in some Europe and has_point_prevalence_range some 1-9 / 100 000 and has_point_prevalence_average_value value 3.0