DiseaseID 11125
额颞叶变性
disease
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 socia
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Disease: 1Symptom: 6Target: 12Links: 18
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 11125
- Core Entity Id
- 68431
- Source Entity Count
- 1
- Preferred Name
- Frontotemporal Lobar Degeneration
- Name Cn
- 额颞叶变性
- Name Pinyin
- E Nie Ye Bian Xing
- Name En
- Frontotemporal Lobar Degeneration
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Mental or Behavioral Dysfunction
- Disgenet Type
- disease
- Mesh Class
- Nervous System Diseases; Mental Disorders; Nutritional and Metabolic Diseases
- Do Class
- Hpo Class
- Mesh Class Name
- Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders
- Hpo Class Name
- Do Class Name
- Disease Definition
- 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.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Frontotemporal Lobar Degeneration
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS011151
Me Sh
D057174
Umls
C0751072
Sym Map
SMDE08859
Dis Ge Net
C0751072
Umls Sty
T048
Me Sh Class
C10C18F03
Tcmbank Disease
4922
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Disease Type
disease
Umls Disease Type
Mental or Behavioral Dysfunction
Disease Definition
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.
Me Sh Disease Class
Nervous System Diseases; Mental Disorders; Nutritional and Metabolic Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders
Umls Semantic Type Name
Mental or Behavioral Dysfunction