Disease #00522
Official abbreviation |
617228 |
Name |
Combined oxidative phosphorylation deficiency 31, 617228 (3) |
OMIM ID |
617228 |
Human Phenotype Ontology Project (HPO) |
HPO |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
MIPEP |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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