autosomal recessive spinocerebellar ataxia 13 (Q21124572)
Jump to navigation
Jump to search
Human disease
- Autosomal recessive spinocerebellar ataxia type 13
- SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13
- SCAR13
- Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency
- Spinocerebellar Ataxia, Autosomal Recessive type 13
- SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13; SCAR13
- Autosomal recessive congenital cerebellar ataxia due to metabotropic glutamate receptor 1 deficiency
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | autosomal recessive spinocerebellar ataxia 13 |
Human disease |
|
Statements
1 reference
1 reference
Identifiers
1 reference
1 reference
1 reference
1 reference
1 reference