Disease #03079 (COQ10D4;SCAR9 (coenzyme Q10 deficiency, primary, type 4), OMIM:612016)
| Official abbreviation |
COQ10D4;SCAR9 |
| Name |
coenzyme Q10 deficiency, primary, type 4 |
| OMIM ID |
612016 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
4 |
| Phenotype entries for this disease |
3 |
| Associated with 1 gene |
ADCK3 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2024-11-08 09:21:06 +01:00 (CET) |
Individuals
|