frontotemporal dementia

Preferred Label : frontotemporal dementia;

MeSH definition : The most common clinical form of FRONTOTEMPORAL LOBAR DEGENERATION, this dementia presents with personality and behavioral changes often associated with disinhibition, apathy, and lack of insight.;

MeSH synonym : dementia, frontotemporal lobe (FLDEM); frontotemporal dementias; frontotemporal lobe dementias (FLDEM); dementia, frontotemporal; dementias, frontotemporal; frontotemporal lobe dementia (FLDEM); dementias, frontotemporal lobe (FLDEM); Wilhelmsen-Lynch disease; frontotemporal lobe dementia; frontotemporal dementia, Ubiquitin-Positive; dementia, Ubiquitin-Positive frontotemporal; dementias, Ubiquitin-Positive frontotemporal; frontotemporal dementia, ubiquitin positive; frontotemporal dementias, Ubiquitin-Positive; Ubiquitin-Positive frontotemporal dementia; Ubiquitin-Positive frontotemporal dementias; frontotemporal lobar degeneration with Ubiquitin-Positive inclusions; dementia, hereditary dysphasic disinhibition; multiple system tauopathy with presenile dementia; frontotemporal dementia with parkinsonism; Disinhibition-Dementia-Parkinsonism-Amyotrophy complex; dementia, frontotemporal, with parkinsonism; complex, Disinhibition-Dementia-Parkinsonism-Amyotrophy; complices, Disinhibition-Dementia-Parkinsonism-Amyotrophy; disinhibition dementia parkinsonism amyotrophy complex; Disinhibition-Dementia-Parkinsonism-Amyotrophy complices; Disinhibition-Dementia-Parkinsonism-Amytrophy complex; complex, Disinhibition-Dementia-Parkinsonism-Amytrophy; complices, Disinhibition-Dementia-Parkinsonism-Amytrophy; disinhibition dementia parkinsonism amytrophy complex; Disinhibition-Dementia-Parkinsonism-Amytrophy complices; familial pick's disease; disease, familial pick's; diseases, familial pick's; familial pick disease; familial pick's diseases; familial picks disease; pick's disease, familial; pick's diseases, familial; frontotemporal dementia with Parkinsonism-17; frontotemporal dementia with parkinsonism 17; frontotemporal lobar degeneration with ubiquitin positive inclusions; dementia, frontotemporal lobe; dementias, frontotemporal lobe; frontotemporal lobe dementias; lobe dementia, frontotemporal; lobe dementias, frontotemporal; FTDP-17; disease, Wilhelmsen-Lynch; diseases, Wilhelmsen-Lynch; wilhelmsen lynch disease; Wilhelmsen-Lynch diseases; GRN-Related frontotemporal dementia; dementia, GRN-Related frontotemporal; dementias, GRN-Related frontotemporal; frontotemporal dementia, GRN-Related; frontotemporal dementias, GRN-Related; GRN related frontotemporal dementia; GRN-Related frontotemporal dementias; hereditary dysphasic disinhibition dementia; FTD-GRN; FTD-PGRN; FTLD-17 GRN; FTLD with TDP-43 pathology; FTLD with TDP 43 pathology; FTLD-TDP; HDDD1; HDDD2; DDPAC;

CISMeF synonym : Ftdp17;

Wikipedia automatic translation : Frontotemporal lobar degeneration;

MeSH hyponym : semantic dementia; Dementia, Semantic; Dementias, Semantic; Semantic Dementias;

Wikipedia link : https://en.wikipedia.org/wiki/Frontotemporal lobar degeneration;

Details

Origin ID

D057180;

UMLS CUI

C0338451;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Frontotemporal dementia [ICD-10 Sub-category]
- Frontotemporal dementia [ICD-9 code]
- Frontotemporal dementia with parkinsonism [ICD-11 More detail]
- Frontotemporal dementia with parkinsonism-17 (disorder) [SNOMED CT concept]
- Frontotemporal dementia, semantic variant [ICD-11 More detail]
- GRN-related frontotemporal dementia (disorder) [SNOMED CT concept]
- MAPT wt Allele [NCIt concept]
- Semantic dementia [PASCAL descriptor]
- Semantic dementia [ORDO Disease]
- Semantic dementia (disorder) [SNOMED CT concept]
- microtubule associated protein tau [ORDO Gene]
Currated CISMeF NLP mapping
- Frontotemporal Dementia [NCIt concept]
- Frontotemporal dementia [PASCAL descriptor]
- Frontotemporal dementia [ICD-11 Category]
- Frontotemporal dementia [HPO term]
- Frontotemporal dementia [OMIM Phenotype]
- Frontotemporal dementia [MedDRA Preferred Term]
- Frontotemporal dementia [ORDO Disease]
- Frontotemporal dementia (disorder) [SNOMED CT concept]
- frontotemporal dementia [DO Concept]
- frontotemporal dementia [Disease (Nov.)]
- frontotemporal dementia [Radlex concept]
DO Cross reference
- frontotemporal dementia [DO Concept]
HPO term
- Frontotemporal dementia [HPO term]
- Semantic dementia [HPO term]
Manual NTBT mappings (CISMeF)
- Frontotemporal degeneration with dementia [ORDO Disease]
- Rare dementia [ORDO Disease]
- Tauopathy with non-Alzheimer non-Pick frontal lobe degeneration [ORDO Disease]
ORDO relation(s)
- Frontotemporal dementia [ORDO Disease]
Record concept(s)
- frontotemporal dementia [MeSH concept]
- semantic dementia [MeSH concept]
Related MeSH Supplementary Concept(s)
- Chromosome 3-Linked Frontotemporal Dementia [MeSH Supplementary Concept]
- amyotrophic lateral sclerosis 6, autosomal recessive [MeSH Supplementary Concept]
- frontotemporal dementia with motor neuron disease [MeSH Supplementary Concept]
- inclusion body myopathy with Early-Onset paget disease and frontotemporal dementia [MeSH Supplementary Concept]
- pallidopontonigral degeneration [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Frontotemporal Dementia [NCIt concept]
- Frontotemporal dementia [MedDRA Preferred Term]
- Frontotemporal dementia [ICD-9 code]
- Frontotemporal dementia [OMIM Phenotype]
- Frontotemporal dementia [ORDO Disease]
- Frontotemporal dementia [ICD-10 Sub-category]
- Frontotemporal dementia [HPO term]
- Frontotemporal dementia [PASCAL descriptor]
- Frontotemporal dementia (disorder) [SNOMED CT concept]
- frontotemporal dementia [Radlex concept]
- frontotemporal dementia [Disease (Nov.)]
Validated automatic mappings to BTNT
- Frontotemporal lobar degeneration with tdp43 inclusions, grn-related [OMIM Phenotype]
- Frontotemporal lobar degeneration with ubiquitin positive inclusions [Disease (Nov.)]
- Semantic dementia [HPO term]

Keyword's position in hierarchy(ies) :

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