DiseaseID 6073
朊病毒病
disease
MSH2017_2016_08_12:A group of genetic, infectious, or sporadic degenerative human and animal nervous system disorders associated with abnormal PRIONS. These diseases are characterized by conversion of the normal prion pr
Relationship Network
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Disease: 1Symptom: 2Target: 12Links: 14
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 6073
- Core Entity Id
- 62670
- Source Entity Count
- 1
- Preferred Name
- Prion Diseases
- Name Cn
- 朊病毒病
- Name Pinyin
- Ruan Bing Du Bing
- Name En
- Prion Diseases
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Infections; Nervous System Diseases
- Do Class
- disease of anatomical entity
- Hpo Class
- Mesh Class Name
- Infections; Nervous System Diseases
- Hpo Class Name
- Do Class Name
- disease of anatomical entity
- Disease Definition
- MSH2017_2016_08_12:A group of genetic, infectious, or sporadic degenerative human and animal nervous system disorders associated with abnormal PRIONS. These diseases are characterized by conversion of the normal prion protein to an abnormal configuration via a post-translational process. In humans, these conditions generally feature DEMENTIA; ATAXIA; and a fatal outcome. Pathologic features include a spongiform encephalopathy without evidence of inflammation. The older literature occasionally refers to these as unconventional SLOW VIRUS DISEASES. (From Proc Natl Acad Sci USA 1998 Nov 10;95(23):13363-83)|CSP2006:any of various brain diseases in humans and animals in which areas of the brain slowly degenerate and take on a spongy appearance.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Prion Diseases
Role
preferred
Name
Human Transmissible Spongiform Encephalopathies, Inherited
Role
preferred
Name
Spongiform Encephalopathy
Role
preferred
Name
Prion Disease
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS004129HBDIS011398HBDIS025985
Me Sh
D017096
Umls
C0162534
Icd10
A81.9
Sym Map
SMDE12457
Do Class
DOID:7
Dis Ge Net
C0162534C0751645C4281802
Umls Sty
T047
Me Sh Class
C01C10
Tcmbank Disease
220322965980
Itcmdb Generated
ITX-DISEASE-E8C0027DEA4C
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Do Class Name
disease of anatomical entity
Disease Type
diseasegroup
Do Disease Class
disease of anatomical entity
Umls Disease Type
Disease or Syndrome
Disease Definition
MSH2017_2016_08_12:A group of genetic, infectious, or sporadic degenerative human and animal nervous system disorders associated with abnormal PRIONS. These diseases are characterized by conversion of the normal prion protein to an abnormal configuration via a post-translational process. In humans, these conditions generally feature DEMENTIA; ATAXIA; and a fatal outcome. Pathologic features include a spongiform encephalopathy without evidence of inflammation. The older literature occasionally refers to these as unconventional SLOW VIRUS DISEASES. (From Proc Natl Acad Sci USA 1998 Nov 10;95(23):13363-83)|CSP2006:any of various brain diseases in humans and animals in which areas of the brain slowly degenerate and take on a spongy appearance.
Me Sh Disease Class
Infections; Nervous System Diseases
Dis Ge Net Disease Type
diseasegroup
Disease Class Name Me Sh
Infections; Nervous System Diseases
Umls Semantic Type Name
Disease or Syndrome