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
This is just here as a test because I lose it
Term information
database
cross reference
- UMLS:C0338451 (E (Exact mapping: the two concepts are equivalent))
- MeSH:D057180 (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))
- ICD-10:G31.0 (- NTBT (ORPHA code's Narrower Term maps to a Broader Term). - Attributed (The ICD10 code is attributed by Orphanet).)
- OMIM:607485 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
- MedDRA:10068968 (E (Exact mapping: the two concepts are equivalent))
- OMIM:600795 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
definition citation
- Orphanet
expertlink
- https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=282
hasDbXref
- OMIM:600274
- ICD-10:G31.0
- OMIM:600795
- OMIM:607485
- MedDRA:10068968
- OMIM:172700
- MeSH:D057180
- UMLS:C0338451
has age of onset
- http://www.orpha.net/ORDO/Orphanet_409948
has annual incidence range
- http://www.orpha.net/ORDO/Orphanet_409977
has inheritance
- http://www.orpha.net/ORDO/Orphanet_409929
has point prevalence range
- http://www.orpha.net/ORDO/Orphanet_409977
notation
- ORPHA:282
- Clinical group
present in
- http://www.orpha.net/ORDO/Orphanet_410100
- http://www.orpha.net/ORDO/Orphanet_409984