spinocerebellar ataxia, autosomal recessive 3

Preferred Label : spinocerebellar ataxia, autosomal recessive 3;

MeSH synonym : spinocerebellar ataxia with blindness and deafness;

Origin ID

C537309;

UMLS CUI

C1849094;

CISMeF manual mappings
- Autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome [ORDO Disease]
Currated CISMeF NLP mapping
- Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) [SNOMED CT concept]
- Spinocerebellar ataxia, autosomal recessive 3 [OMIM Phenotype]
- autosomal recessive spinocerebellar ataxia 3 [DO Concept]
DO Cross reference
- autosomal recessive spinocerebellar ataxia 3 [DO Concept]
MeSH term(s) associated for indexing
- spinocerebellar degenerations [MeSH Descriptor]
Record concept(s)
- Spinocerebellar ataxia, autosomal recessive 3 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) [SNOMED CT concept]
- Autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome [ORDO Disease]
- Spinocerebellar ataxia, autosomal recessive 3 [OMIM Phenotype]
- autosomal recessive spinocerebellar ataxia 3 [DO Concept]