Disease #05066 (SCAR-12 (ataxia, spinocerebellar, autosomal recessive, type 12 (SCAR12)), OMIM:614322)
Official abbreviation |
SCAR-12 |
Name |
ataxia, spinocerebellar, autosomal recessive, type 12 (SCAR12) |
OMIM ID |
614322 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
WWOX |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|
|