DiseaseID 4720
神经变性
disease
MSH2017_2016_08_12:Loss of functional activity and trophic degeneration of nerve axons and their terminal arborizations following the destruction of their cells of origin or interruption of their continuity with these ce
Relationship Network
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Disease: 1Symptom: 12Target: 12Links: 24
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 4720
- Core Entity Id
- 61110
- Source Entity Count
- 2
- Preferred Name
- Nerve Degeneration
- Name Cn
- 神经变性
- Name Pinyin
- Shen Jing Bian Xing
- Name En
- Nerve Degeneration
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Cell or Molecular Dysfunction
- Disgenet Type
- disease
- Mesh Class
- Nervous System DiseasesPathological Conditions, Signs and Symptoms
- Do Class
- disease of anatomical entity
- Hpo Class
- Abnormality of the nervous system
- Mesh Class Name
- Nervous System DiseasesPathological Conditions, Signs and Symptoms
- Hpo Class Name
- Abnormality of the nervous system
- Do Class Name
- disease of anatomical entity
- Disease Definition
- MSH2017_2016_08_12:Loss of functional activity and trophic degeneration of nerve axons and their terminal arborizations following the destruction of their cells of origin or interruption of their continuity with these cells. The pathology is characteristic of neurodegenerative diseases. Often the process of nerve degeneration is studied in research on neuroanatomical localization and correlation of the neurophysiology of neural pathways.|HPO2016_07_04:Progressive loss of neural cells and tissue. [HPO:probinson]|CSP2006:loss of functional activity and trophic degeneration of nerve axons and their terminal arborizations following the destruction of their cells of origin or interruption of their continuity with these cells.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Nerve Degeneration
Role
preferred
Name
Neurodegenerative Disorders
Role
preferred
Name
Degenerative Diseases, Central Nervous System
Role
preferred
Name
Degenerative Diseases, Spinal Cord
Role
preferred
Name
Degenerative Disorder
Role
preferred
Name
Neuro-Degenerative Disease
Role
preferred
Name
Degenerative Disease of Nervous System, Unspecified
Role
alias
Name
Neurodegeneration
Role
alias
Name
Neurodegenerative Diseases
Role
alias
Name
Progressive Neurodegenerative Disorder
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0002180
Herb
ETCM3110HBDIS002097HBDIS006480HBDIS009980HBDIS011436HBDIS013207HBDIS023501
Me Sh
D009410D019636
Umls
C0027746C0524851
Icd10
G31.9
Sym Map
SMDE11389SMDE11430
Do Class
DOID:7
Dis Ge Net
C0027746C0270715C0524851C0751733C1285162C4020854
Umls Sty
T047T049
Hpo Class
HP:0000707
Me Sh Class
C10C23
Tcmbank Disease
121191362917409294913245149926932
Itcmdb Generated
ITX-DISEASE-58C556D0A572
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Do Class Name
disease of anatomical entity
Disease Type
diseasegroupphenotype
Hpo Class Name
Abnormality of the nervous system
Do Disease Class
disease of anatomical entity
Hpo Disease Class
Abnormality of the nervous system
Umls Disease Type
Cell or Molecular DysfunctionDisease or Syndrome
Disease Definition
MSH2017_2016_08_12:Loss of functional activity and trophic degeneration of nerve axons and their terminal arborizations following the destruction of their cells of origin or interruption of their continuity with these cells. The pathology is characteristic of neurodegenerative diseases. Often the process of nerve degeneration is studied in research on neuroanatomical localization and correlation of the neurophysiology of neural pathways.|HPO2016_07_04:Progressive loss of neural cells and tissue. [HPO:probinson]|CSP2006:loss of functional activity and trophic degeneration of nerve axons and their terminal arborizations following the destruction of their cells of origin or interruption of their continuity with these cells.PSY2004:Neurologic disorders characterized by progressive nervous system dysfunction and loss of neural tissue.|MSH2017_2016_08_12:Hereditary and sporadic conditions which are characterized by progressive nervous system dysfunction. These disorders are often associated with atrophy of the affected central or peripheral nervous system structures.|LNC256:Neurodegenerative disorders, such as Hunter syndrome, or sensory motor neuropathies, such as Friedreich ataxia and Charcot-Marie-Tooth syndrome.
Me Sh Disease Class
Nervous System DiseasesPathological Conditions, Signs and Symptoms
Dis Ge Net Disease Type
diseasegroupphenotype
Disease Class Name Me Sh
Nervous System DiseasesPathological Conditions, Signs and Symptoms
Umls Semantic Type Name
Cell or Molecular DysfunctionDisease or Syndrome