Disease #03079 (COQ10D-4;SCAR-9 (coenzyme Q10 deficiency, primary, type 4 (COQ10D-4, spinocerebellar ataxia, autosomal recessive, type 9 (SCAR-9))), OMIM:612016)
| Official abbreviation |
COQ10D-4;SCAR-9 |
| Name |
coenzyme Q10 deficiency, primary, type 4 (COQ10D-4, spinocerebellar ataxia, autosomal recessive, type 9 (SCAR-9)) |
| OMIM ID |
612016 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
ADCK3 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
|
