ataxia, spastic, 3, autosomal recessive

Preferred Label : ataxia, spastic, 3, autosomal recessive;

MeSH synonym : autosomal recessive spastic ataxia with leukoencephalopathy;

Origin ID

C566956;

UMLS CUI

C1969645;

Currated CISMeF NLP mapping
- Autosomal recessive spastic ataxia with leukoencephalopathy [ORDO Disease]
- Autosomal recessive spastic ataxia with leukoencephalopathy (disorder) [SNOMED CT concept]
- Spastic ataxia 3, autosomal recessive [OMIM Phenotype]
MeSH term(s) associated for indexing
- cerebellar ataxia [MeSH Descriptor]
- leukoencephalopathies [MeSH Descriptor]
- spastic paraplegia, hereditary [MeSH Descriptor]
Record concept(s)
- ataxia, spastic, 3, autosomal recessive [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal recessive spastic ataxia with leukoencephalopathy [ORDO Disease]
- Autosomal recessive spastic ataxia with leukoencephalopathy (disorder) [SNOMED CT concept]
- Spastic ataxia 3, autosomal recessive [OMIM Phenotype]