DiseaseID 4763
橄榄体脑桥小脑萎缩
disease
NCI2016_02D:A group of sporadic and inherited neurodegenerative disorders affecting the cerebellum, pons, and inferior olives.|MSH2017_2016_08_12:A group of inherited and sporadic disorders which share progressive ataxia
Relationship Network
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Disease: 1Symptom: 1Target: 12Links: 13
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 4763
- Core Entity Id
- 61161
- Source Entity Count
- 1
- Preferred Name
- Olivopontocerebellar Atrophies
- Name Cn
- 橄榄体脑桥小脑萎缩
- Name Pinyin
- Gan Lan Ti Nao Qiao Xiao Nao Wei Suo
- Name En
- Olivopontocerebellar Atrophies
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
- Do Class
- disease of anatomical entity
- Hpo Class
- Abnormality of the nervous system
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
- Hpo Class Name
- Abnormality of the nervous system
- Do Class Name
- disease of anatomical entity
- Disease Definition
- NCI2016_02D:A group of sporadic and inherited neurodegenerative disorders affecting the cerebellum, pons, and inferior olives.|MSH2017_2016_08_12:A group of inherited and sporadic disorders which share progressive ataxia in combination with atrophy of the CEREBELLUM; PONS; and inferior olivary nuclei. Additional clinical features may include MUSCLE RIGIDITY; NYSTAGMUS, PATHOLOGIC; RETINAL DEGENERATION; MUSCLE SPASTICITY; DEMENTIA; URINARY INCONTINENCE; and OPHTHALMOPLEGIA. The familial form has an earlier onset (second decade) and may feature spinal cord atrophy. The sporadic form tends to present in the fifth or sixth decade, and is considered a clinical subtype of MULTIPLE SYSTEM ATROPHY. (From Adams et al., Principles of Neurology, 6th ed, p1085)|HPO2016_07_04:Neuronal degeneration in the cerebellum, pontine nuclei, and inferior olivary nucleus. [HPO:probinson]
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Olivopontocerebellar Atrophies
Role
preferred
Name
Familial Olivopontocerebellar Atrophy
Role
preferred
Name
Olivopontocerebellar Atrophy
Role
alias
Name
Olivopontocerebellar Degeneration
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0002542
Herb
HBDIS002170HBDIS011277
Me Sh
D009849
Umls
C0028968
Sym Map
SMDE11600
Do Class
DOID:7
Dis Ge Net
C0028968C0751398
Umls Sty
T047
Hpo Class
HP:0000707
Me Sh Class
C10C16
Tcmbank Disease
166885077
Itcmdb Generated
ITX-DISEASE-D31FBC79A4C4
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Do Class Name
disease of anatomical entity
Disease Type
diseasegroup
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
Disease or Syndrome
Disease Definition
NCI2016_02D:A group of sporadic and inherited neurodegenerative disorders affecting the cerebellum, pons, and inferior olives.|MSH2017_2016_08_12:A group of inherited and sporadic disorders which share progressive ataxia in combination with atrophy of the CEREBELLUM; PONS; and inferior olivary nuclei. Additional clinical features may include MUSCLE RIGIDITY; NYSTAGMUS, PATHOLOGIC; RETINAL DEGENERATION; MUSCLE SPASTICITY; DEMENTIA; URINARY INCONTINENCE; and OPHTHALMOPLEGIA. The familial form has an earlier onset (second decade) and may feature spinal cord atrophy. The sporadic form tends to present in the fifth or sixth decade, and is considered a clinical subtype of MULTIPLE SYSTEM ATROPHY. (From Adams et al., Principles of Neurology, 6th ed, p1085)|HPO2016_07_04:Neuronal degeneration in the cerebellum, pontine nuclei, and inferior olivary nucleus. [HPO:probinson]
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Dis Ge Net Disease Type
diseasegroup
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Umls Semantic Type Name
Disease or Syndrome