Term ID: | 10510 |
Name: | Spinocerebellar Ataxia 31 |
Definition: | |
Alternative IDs: | OMIM:117210 |
ParentIDs: | MESH:D020754 |
TreeNumbers: | C10.228.140.252.190.530/C566146 |C10.228.140.252.700.700/C566146 |C10.228.854.787.875/C566146 |C10.574.500.825.700/C566146 |C10.597.350.090.500.530/C566146 |C16.320.400.780.875/C566146 |
Synonyms: | SCA31 |Spinocerebellar Ataxia, 16q22-Linked |
Slim Mappings: | Genetic disease (inborn)|Nervous system disease |
Reference: |
MedGen: C566146
MeSH: C566146
OMIM: 117210;
Genes: BEAN1; |
Phenotypes | |
Disease Causing ClinVar Variants | |