Disease #00564
Official abbreviation |
617873 |
Name |
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 35 |
OMIM ID |
617873 |
Human Phenotype Ontology Project (HPO) |
HPO |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
TRIT1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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