autosomal recessive spinocerebellar ataxia 18 (Q21124560)
Jump to navigation
Jump to search
Human disease
- SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18; SCAR18
- SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18
- Autosomal recessive congenital cerebellar ataxia due to GRID2 deficiency
- Autosomal recessive congenital cerebellar ataxia due to ionotropic glutamate receptor delta-2 subunit deficiency
- Spinocerebellar Ataxia, Autosomal Recessive type 18
- SCAR18
- autosomal recessive spinocerebellar ataxia type 18
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | autosomal recessive spinocerebellar ataxia 18 |
Human disease |
|
Statements
1 reference
1 reference
Identifiers
1 reference
1 reference
1 reference
1 reference
1 reference