Dataset | HPO Gene-Disease Associations |
Category | disease or phenotype associations |
Type | phenotype |
Description | An anomaly in the surface contour of mitochondria. (Human Phenotype Ontology, HP_0012087) |
External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0012087 |
Similar Terms | |
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1 genes associated with the abnormal mitochondrial shape phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Symbol | Name |
---|---|
SLC25A3 | solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 3 |