Disease #00010
Official abbreviation |
615228 |
Name |
Mitochondrial complex (ATP synthase) deficiency, nuclear type 4, 615228 (3) |
OMIM ID |
615228 |
Human Phenotype Ontology Project (HPO) |
HPO |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 2 genes |
ATP5A1, ATP5F1A |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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