Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.
Core Information
Disease Name
Frontotemporal Lobar Degeneration
Standard Disease Name
frontotemporal lobar degeneration
MeSH Tree
No data
ICD-10
No data
Identifiers
DO ID
No data
MeSH ID
D057174
OMIM ID
No data
UMLS ID
C0751072
HPO ID
No data
Description and Extensions
Description
MSH2017_2016_08_12:Heterogeneous group of neurodegenerative disorders characterized by frontal and temporal lobe atrophy associated with neuronal loss, gliosis, and dementia. Patients exhibit progressive changes in social, behavioral, and/or language function. Multiple subtypes or forms are recognized based on presence or absence of TAU PROTEIN inclusions. FTLD includes three clinical syndromes: FRONTOTEMPORAL DEMENTIA, semantic dementia, and PRIMARY PROGRESSIVE NONFLUENT APHASIA.
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.