abnormal mitochondrial morphology Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Any structural anomaly of the mitochondria. (Human Phenotype Ontology, HP_0008322)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008322
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Genes

2 genes associated with the abnormal mitochondrial morphology 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
TAZ tafazzin