Preferred Name

Frontotemporal Dementia [Disease/Finding]

Synonyms

Hereditary Dysphasic Disinhibition Dementia

FTDP-17

ID

http://purl.bioontology.org/ontology/NDFRT/N0000181125

altLabel

Hereditary Dysphasic Disinhibition Dementia

Frontotemporal Lobar Degeneration With Ubiquitin-Positive Inclusions

DDPAC

Frontotemporal Dementia

FTD-PGRN

Disinhibition-Dementia-Parkinsonism-Amytrophy Complex

Frontotemporal Lobe Dementia

Dementia, Frontotemporal, with Parkinsonism

Frontotemporal Dementia, Ubiquitin-Positive

Frontotemporal Lobe Dementia (FLDEM)

FTLD with TDP-43 Pathology

Wilhelmsen-Lynch Disease

Frontotemporal Dementia with Parkinsonism

FTLD-17 GRN

HDDD2

FTLD-TDP

Frontotemporal Dementia with Parkinsonism-17

FTD-GRN

HDDD1

Dementia, Frontotemporal

Familial Pick's Disease

GRN-Related Frontotemporal Dementia

Multiple System Tauopathy with Presenile Dementia

Disinhibition-Dementia-Parkinsonism-Amyotrophy Complex

Dementia, Hereditary Dysphasic Disinhibition

FTDP-17

cui

C0338451

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 DUI

D057180

MeSH name

Frontotemporal Dementia

MESH UI

M0534991

NDFRT kind

DISEASE_KIND

notation

N0000181125

NUI

N0000181125

prefLabel

Frontotemporal Dementia [Disease/Finding]

tui

T047

subClassOf

http://purl.bioontology.org/ontology/NDFRT/N0000181173

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