|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An anomaly in the surface contour of mitochondria. (Human Phenotype Ontology, HP_0012087)|
|Downloads & Tools|
1 genes associated with the abnormal mitochondrial shape phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|SLC25A3||solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 3|