| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| External Link | http://www.omim.org/entry/611719 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the combined oxidative phosphorylation deficiency 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| MRPS22 | mitochondrial ribosomal protein S22 |
