Spinocerebellar ataxia, autosomal recessive 10

Preferred Label : Spinocerebellar ataxia, autosomal recessive 10;

CISMeF synonym : spinocerebellar ataxia, autosomal recessive 3;

MeSH synonym : spinocerebellar ataxia with blindness and deafness; Spinocerebellar ataxia, autosomal recessive 3; Autosomal recessive spinocerebellar ataxia type 10; autosomal recessive spinocerebellar ataxia type 10 (SCAR10);

Details

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
- Brown-Vialetto-Van Laere syndrome 2 [DO Concept]
- Peroxisome biogenesis disorder 4B [DO Concept]
- autosomal recessive spinocerebellar ataxia 3 [DO Concept]
MeSH term(s) associated for indexing
- spinocerebellar ataxias [MeSH Descriptor]
- spinocerebellar degenerations [MeSH Descriptor]
ORDO relation(s)
- Autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome [ORDO Disease]
Record concept(s)
- Spinocerebellar ataxia, autosomal recessive 10 [MeSH concept]
See also inter- (CISMeF)
- Brown-Vialetto-Van Laere syndrome 2 [DO 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]

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