spinocerebellar ataxia, autosomal recessive, with axonal neuropathy

Preferred Label : spinocerebellar ataxia, autosomal recessive, with axonal neuropathy;

Origin ID

C537313;

UMLS CUI

C1846574;

Automatic exact mappings (from CISMeF team)
- Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy [OMIM phenotypic series]
Currated CISMeF NLP mapping
- Spinocerebellar ataxia with axonal neuropathy type 1 [ORDO Disease]
- Spinocerebellar ataxia with axonal neuropathy type 1 (disorder) [SNOMED CT concept]
- Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1 [OMIM Phenotype]
- spinocerebellar ataxia type 1 with axonal neuropathy [DO Concept]
MeSH term(s) associated for indexing
- spinocerebellar degenerations [MeSH Descriptor]
Record concept(s)
- Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy [MeSH concept]
See also inter- (CISMeF)
- Spinocerebellar ataxia with axonal neuropathy type 1 [ORDO Disease]
- Spinocerebellar ataxia with axonal neuropathy type 2 [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Spinocerebellar ataxia with axonal neuropathy type 1 [ORDO Disease]
- Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1 [OMIM Phenotype]