Disease #01740 (cytochrome-c oxidase deficiency (mitochondrial complex IV deficiency), OMIM:220110)
| Official abbreviation |
- |
| Name |
cytochrome-c oxidase deficiency (mitochondrial complex IV deficiency) |
| OMIM ID |
220110 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 10 genes |
APOPT1, COA5, COX10, COX14, COX20, COX6B1, FASTKD2, PET100, SCO1, TACO1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
|
