Tauopathy
MONDO:0005574Neurodegenerative disorders involving deposition of abnormal tau protein isoforms (tau proteins) in neurons and glial cells in the brain. Pathological aggregations of tau proteins are associated with mutation of the tau gene on chromosome 17 in patients with alzheimer disease; dementia; parkinsonian disorders; progressive supranuclear palsy (supranuclear palsy, progressive); and corticobasal degeneration.
1193 clinical trials for this condition and its sub-types, 24 tagged with Tauopathy itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Tauopathy
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Alzheimer disease 1,187 trials
5 sub-types
- Familial Alzheimer disease 13 trials · 55 incl. sub-types Sub-types →
- Alzheimer disease 16 1 trial
- Alzheimer disease 17 1 trial
- Alzheimer disease 18 1 trial
- Alzheimer disease 19 1 trial
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Argyrophilic grain disease 0 trials
Most studied deeper sub-types
Early-onset autosomal dominant Alzheimer disease
(31)
Alzheimer disease 2
(11)
Alzheimer disease 3
(5)
Alzheimer disease type 1
(4)
Alzheimer disease 4
(3)
Alzheimer disease 10
(1)
Alzheimer disease 11
(1)
Alzheimer disease 12
(1)
Alzheimer disease 13
(1)
Alzheimer disease 14
(1)
Alzheimer disease 5
(1)
Alzheimer disease 6
(1)
Alzheimer disease 7
(1)
Alzheimer disease 8
(1)
Alzheimer disease without neurofibrillary tangles
(1)
Alzheimer disease, familial early-onset, with coexisting amyloid and prion pathology
(0)