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Diseases

Frontotemporal Lobar Degeneration

frontotemporal lobar degeneration

Entity Type
Diseases
Relation Groups
3
Relation Preview
24

Basic Information

Grouped by core information, identifiers, and descriptions.

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

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
02
CDK5R1
cyclin dependent kinase 5 regulatory subunit 1
cyclin dependent kinase 5 regulatory subunit 1
04
MAPT
microtubule associated protein tau
microtubule associated protein tau