Disease #03546 (COXPD-8 (combined oxidative phosphorylation deficiency, type 8 (COXPD-8)), OMIM:614096)
| Official abbreviation |
COXPD-8 |
| Name |
combined oxidative phosphorylation deficiency, type 8 (COXPD-8) |
| OMIM ID |
614096 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
AARS2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
|
