Disease #04419 (CEMCOX-3 (cardioencephalomyopathy?, fatal infantile, due to cytochrome C oxidase deficiency, type 3 (CEMCOX-3)), OMIM:616500)
| Official abbreviation |
CEMCOX-3 |
| Name |
cardioencephalomyopathy?, fatal infantile, due to cytochrome C oxidase deficiency, type 3 (CEMCOX-3) |
| OMIM ID |
616500 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
COA5 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 10:25:22 +02:00 (CEST) |
| Date last edited |
N/A |
|
