spinocerebellar ataxia 8

Preferred Label : spinocerebellar ataxia 8;

MeSH synonym : SCA8 Spinocerebellar ataxia 8;

Origin ID

C537307;

UMLS CUI

C1837454;

Automatic exact mappings (from CISMeF team)
- Mitochondrial dna depletion syndrome 7 (hepatocerebral type) [OMIM Phenotype]
CISMeF manual mappings
- Spinocerebellar ataxia type 8 [ORDO Disease]
Currated CISMeF NLP mapping
- Spinocerebellar ataxia 8 [OMIM Phenotype]
- Spinocerebellar ataxia type 8 [ICD-11 More detail]
- Spinocerebellar ataxia type 8 (disorder) [SNOMED CT concept]
- spinocerebellar ataxia 8 [Disease (Nov.)]
- spinocerebellar ataxia type 8 [DO Concept]
MeSH term(s) associated for indexing
- spinocerebellar degenerations [MeSH Descriptor]
ORDO relation(s)
- Spinocerebellar ataxia type 8 [ORDO Disease]
Record concept(s)
- Spinocerebellar ataxia 8 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Spinocerebellar ataxia 8 [OMIM Phenotype]
- Spinocerebellar ataxia type 8 [ORDO Disease]
- Spinocerebellar ataxia type 8 [ICD-11 More detail]
- Spinocerebellar ataxia type 8 (disorder) [SNOMED CT concept]
- spinocerebellar ataxia 8 [Disease (Nov.)]
- spinocerebellar ataxia type 8 [DO Concept]