spinocerebellar ataxia, autosomal recessive 4

Preferred Label : spinocerebellar ataxia, autosomal recessive 4;

MeSH synonym : spinocerebellar ataxia with saccadic intrusions;

Origin ID

C537310;

UMLS CUI

C1846492;

CISMeF manual mappings
- Autosomal recessive cerebellar ataxia-movement disorder syndrome [ORDO Disease]
Currated CISMeF NLP mapping
- Spinocerebellar ataxia, autosomal recessive 4 [OMIM Phenotype]
- autosomal recessive spinocerebellar ataxia 4 [DO Concept]
DO Cross reference
- autosomal recessive spinocerebellar ataxia 4 [DO Concept]
MeSH term(s) associated for indexing
- spinocerebellar degenerations [MeSH Descriptor]
Record concept(s)
- Spinocerebellar ataxia, autosomal recessive 4 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal recessive cerebellar ataxia-movement disorder syndrome [ORDO Disease]
- Spinocerebellar ataxia, autosomal recessive 4 [OMIM Phenotype]
- autosomal recessive spinocerebellar ataxia 4 [DO Concept]