Disease #00847 (COXPD-14 (oxidative phosphorylation deficiency, combined, type 14 (COXPD-14)), OMIM:614946)
| Official abbreviation |
COXPD-14 |
| Name |
oxidative phosphorylation deficiency, combined, type 14 (COXPD-14) |
| OMIM ID |
614946 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
FARS2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
|
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