Disease #03834 (CEMCOX2 (cardioencephalomyopathy, fatal infantile, due to cytochrome C oxidase deficiency, type 2 (CEMCOX-2)), OMIM:615119)
| Official abbreviation |
CEMCOX2 |
| Name |
cardioencephalomyopathy, fatal infantile, due to cytochrome C oxidase deficiency, type 2 (CEMCOX-2) |
| OMIM ID |
615119 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
0 |
| Phenotype entries for this disease |
0 |
| Associated with 1 gene |
COX15 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
|
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