Disease #00482
Official abbreviation |
CEMCOX1 |
Name |
CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 1; CEMCOX1 |
OMIM ID |
604377 |
Human Phenotype Ontology Project (HPO) |
HPO |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
SCO2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|