Tauopathy disease type

General Details:

Name:
Tauopathy disease type
Steward:
NINDS
Definition:
Presence of disease resulting from the pathological aggregation of tau protein
Registration Status:
Qualified

Permissible Values:

Data Type:
Value List
Unit of Measure:
Ids:
Value Code Name Code Code System Code Description
Pick's Disease Pick's Disease Pick's Disease
Corticobasal degeneration Corticobasal degeneration Corticobasal degeneration
Progressive supranuclear palsy Progressive supranuclear palsy Progressive supranuclear palsy
Argyrophilic grain dementia (including diffuse AGD) Argyrophilic grain dementia (including diffuse AGD) Argyrophilic grain dementia (including diffuse AGD)
Other 4R tauopathy (e.g., multisystem tauopathy) Other 4R tauopathy (e.g., multisystem tauopathy) Other 4R tauopathy (e.g., multisystem tauopathy)
Tangle-predominant dementia (including Parkinson dementia complex) Tangle-predominant dementia (including Parkinson dementia complex) Tangle-predominant dementia (including Parkinson dementia complex)

Designations:

Designation:
Tauopathy disease type
Tags:

Designations:

Definition:
Presence of disease resulting from the pathological aggregation of tau protein
Tags:

Reference Documents:

ID:
Title:
URI:
Provider Org:
Language Code:
Document:
DICKSON, D. W. 1998. Pick's disease: a modern approach. Brain Pathol, 8, 339-54. DICKSON, D. W., BERGERON, C., CHIN, S. S., DUYCKAERTS, C., HOROUPIAN, D., IKEDA, K., JELLINGER, K., LANTOS, P. L., LIPPA, C. F., MIRRA, S. S., TABATON, M., VONSATTEL, J. P., WAKABAYASHI, K. & LITVAN, I. 2002. Office of Rare Diseases neuropathologic criteria for corticobasal degeneration. J Neuropathol Exp Neurol, 61, 935-46. LANTOS, P. L. 1994. The neuropathology of progressive supranuclear palsy. J Neural Transm Suppl, 42, 137-52. TOLNAY, M. & CLAVAGUERA, F. 2004. Argyrophilic grain disease: a late-onset dementia with distinctive features among tauopathies. Neuropathology, 24, 269-83. BIGIO, E. H., LIPTON, A. M., YEN, S. H., HUTTON, M. L., BAKER, M., NACHARAJU, P., WHITE, C. L., 3RD, DAVIES, P., LIN, W. & DICKSON, D. W. 2001. Frontal lobe dementia with novel tauopathy: sporadic multiple system tauopathy with dementia. J Neuropathol Exp Neurol, 60, 328-41. KOVACS, G. G., MAJTENYI, K., SPINA, S., MURRELL, J. R., GELPI, E., HOFTBERGER, R., FRASER, G., CROWTHER, R. A., GOEDERT, M., BUDKA, H. & GHETTI, B. 2008. White matter tauopathy with globular glial inclusions: a distinct sporadic frontotemporal lobar degeneration. J Neuropathol Exp Neurol, 67, 963-75. JELLINGER, K. A. & BANCHER, C. 1998. Senile dementia with tangles (tangle predominant form of senile dementia). Brain Pathol, 8, 367-76. HOF, P. R., PERL, D. P., LOERZEL, A. J. & MORRISON, J. H. 1991. Neurofibrillary tangle distribution in the cerebral cortex of parkinsonism-dementia cases from Guam: differences with Alzheimer's disease. Brain Res, 564, 306-13.

Identifiers:

Source:
NLM
Id:
CdyBG9hvE
Version:
Source:
NINDS
Id:
C08196
Version:
3
Source:
BRICS Variable Name
Id:
TaupthyDisTyp
Version: