DiseaseID 5131
亚急性硬化性全脑炎
disease
NCI2016_NICHD_1602D:An encephalitic disorder that occurs following a measles infection. The disease initially manifests as personality changes, and then progresses to muscle spasms and seizures, possibly death.|NCI2016_0
Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
Click a node to open it in a new tab
Disease: 1Target: 11Links: 11
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 5131
- Core Entity Id
- 61582
- Source Entity Count
- 1
- Preferred Name
- Subacute Sclerosing Panencephalitis
- Name Cn
- 亚急性硬化性全脑炎
- Name Pinyin
- Ya Ji Xing Ying Hua Xing Quan Nao Yan
- Name En
- Subacute Sclerosing Panencephalitis
- 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 by infectious agent
- Hpo Class
- Mesh Class Name
- Infections; Nervous System Diseases
- Hpo Class Name
- Do Class Name
- disease by infectious agent
- Disease Definition
- NCI2016_NICHD_1602D:An encephalitic disorder that occurs following a measles infection. The disease initially manifests as personality changes, and then progresses to muscle spasms and seizures, possibly death.|NCI2016_02D:A rare, slowly progressive post-infectious neurological disorder affecting the central nervous system. It is characterized by seizures, ataxia, myoclonus, personality changes, spasticity, and coma. The symptoms appear several years following measles infection at an early age.|MSH2017_2016_08_12:A rare, slowly progressive encephalitis caused by chronic infection with the MEASLES VIRUS. The condition occurs primarily in children and young adults, approximately 2-8 years after the initial infection. A gradual decline in intellectual abilities and behavioral alterations are followed by progressive MYOCLONUS; MUSCLE SPASTICITY; SEIZURES; DEMENTIA; autonomic dysfunction; and ATAXIA. DEATH usually occurs 1-3 years after disease onset. Pathologic features include perivascular cuffing, eosinophilic cytoplasmic inclusions, neurophagia, and fibrous gliosis. It is caused by the SSPE virus, which is a defective variant of MEASLES VIRUS. (From Adams et al., Principles of Neurology, 6th ed, pp767-8)|CSP2006:rare chronic progressive encephalitis caused by the measles virus and occurring primarily in children and young adults; death usually occurs within three years; characterized by primary measles infection before the age of two years.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Subacute Sclerosing Panencephalitis
Role
preferred
Name
Panencephalitis, Subacute Sclerosing
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS002863
Me Sh
D013344
Omim
260470
Umls
C0038522
Icd10
A81.1
Sym Map
SMDE13696
Do Class
DOID:0050117
Dis Ge Net
C0038522
Umls Sty
T047
Me Sh Class
C01C10
Tcmbank Disease
21848
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Do Class Name
disease by infectious agent
Disease Type
disease
Do Disease Class
disease by infectious agent
Umls Disease Type
Disease or Syndrome
Disease Definition
NCI2016_NICHD_1602D:An encephalitic disorder that occurs following a measles infection. The disease initially manifests as personality changes, and then progresses to muscle spasms and seizures, possibly death.|NCI2016_02D:A rare, slowly progressive post-infectious neurological disorder affecting the central nervous system. It is characterized by seizures, ataxia, myoclonus, personality changes, spasticity, and coma. The symptoms appear several years following measles infection at an early age.|MSH2017_2016_08_12:A rare, slowly progressive encephalitis caused by chronic infection with the MEASLES VIRUS. The condition occurs primarily in children and young adults, approximately 2-8 years after the initial infection. A gradual decline in intellectual abilities and behavioral alterations are followed by progressive MYOCLONUS; MUSCLE SPASTICITY; SEIZURES; DEMENTIA; autonomic dysfunction; and ATAXIA. DEATH usually occurs 1-3 years after disease onset. Pathologic features include perivascular cuffing, eosinophilic cytoplasmic inclusions, neurophagia, and fibrous gliosis. It is caused by the SSPE virus, which is a defective variant of MEASLES VIRUS. (From Adams et al., Principles of Neurology, 6th ed, pp767-8)|CSP2006:rare chronic progressive encephalitis caused by the measles virus and occurring primarily in children and young adults; death usually occurs within three years; characterized by primary measles infection before the age of two years.
Me Sh Disease Class
Infections; Nervous System Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Infections; Nervous System Diseases
Umls Semantic Type Name
Disease or Syndrome