spinocerebellar ataxia, autosomal recessive 7

Preferred Label : spinocerebellar ataxia, autosomal recessive 7;

MeSH synonym : Spinocerebellar Ataxia Autosomal Recessive 7; SCAR7 Spinocerebellar Ataxia Autosomal Recessive 7;

Details

Origin ID

C563753;

UMLS CUI

C1836474;

Currated CISMeF NLP mapping
- Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia [ORDO Disease]
- Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia (disorder) [SNOMED CT concept]
- Spinocerebellar ataxia, autosomal recessive 7 [OMIM Phenotype]
- autosomal recessive spinocerebellar ataxia 7 [DO Concept]
MeSH term(s) associated for indexing
- spinocerebellar ataxias [MeSH Descriptor]
Record concept(s)
- spinocerebellar ataxia, autosomal recessive 7 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia [ORDO Disease]
- Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia (disorder) [SNOMED CT concept]
- Spinocerebellar ataxia, autosomal recessive 7 [OMIM Phenotype]
- autosomal recessive spinocerebellar ataxia 7 [DO Concept]

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