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Diseases
Olivopontocerebellar Atrophies
olivopontocerebellar atrophies
- Entity Type
- Diseases
- Relation Groups
- 3
- Relation Preview
- 24
Basic Information
Grouped by core information, identifiers, and descriptions.
Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.
Core Information
- Disease Name
- Olivopontocerebellar Atrophies
- Standard Disease Name
- olivopontocerebellar atrophies
- MeSH Tree
- No data
- ICD-10
- No data
Identifiers
- DO ID
- No data
- MeSH ID
- D009849
- OMIM ID
- MTHU015558|MTHU016549
- UMLS ID
- C0028968
- HPO ID
- No data
Description and Extensions
- Description
- 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]
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.
Candidate Ingredients
target disease -> ingredient target8 Ingredients