Olivopontocerebellar Atrophy

Preferred Label : Olivopontocerebellar Atrophy;

NCIt definition : A group of sporadic and inherited neurodegenerative disorders affecting the cerebellum, pons, and inferior olives.;

Details

Origin ID

C84947;

UMLS CUI

C0028968;

Automatic exact mappings (from CISMeF team)
- Spinocerebellar ataxia 1 [OMIM Phenotype]
- Spinocerebellar ataxia 7 [OMIM Phenotype]
- spinocerebellar ataxias [MeSH Descriptor]
Currated CISMeF NLP mapping
- Olivopontocerebellar atrophy [MedDRA LLT]
- Olivopontocerebellar atrophy [ICD-11 More detail]
- Olivopontocerebellar atrophy [HPO term]
- Olivopontocerebellar degeneration (disorder) [SNOMED CT concept]
- olivocerebellar atrophy [SNOMED Notion]
- olivopontocerebellar atrophies [MeSH Descriptor]
- olivopontocerebellar atrophies [MeSH concept]
- olivopontocerebellar atrophy [DO Concept]
- olivopontocerebellar degeneration [SNOMED Notion]
- olivopontocerebellar degeneration [Radlex concept]
DO Cross reference
- olivopontocerebellar atrophy [DO Concept]
Has associated anatomic sites
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Olivopontocerebellar atrophy [MedDRA LLT]
- Olivopontocerebellar atrophy [HPO term]
- Olivopontocerebellar degeneration (disorder) [SNOMED CT concept]
- olivocerebellar atrophy [SNOMED Notion]
- olivopontocerebellar atrophies [MeSH concept]
- olivopontocerebellar atrophies [MeSH Descriptor]
- olivopontocerebellar atrophy [DO Concept]
- olivopontocerebellar degeneration [Radlex concept]
- olivopontocerebellar degeneration [SNOMED Notion]
Validated automatic mappings to BTNT
- Olivopontocerebellar atrophy V [OMIM Phenotype]
- Spinocerebellar ataxia 2 [OMIM Phenotype]
disease_has_finding
- Rare Lesion [NCIt concept]

Keyword's position in hierarchy(ies) :

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