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