Source: UNIPROT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1355
Gene Symbol: COX15
COX15
CUI: C0023264
Disease: Leigh Disease
Leigh Disease 		0.740 GeneticVariation UNIPROT Only two COX15 mutated patients, one with severe neonatal cardiomyopathy, the other with rapidly fatal Leigh syndrome, have been described to date. 15863660

2005
Entrez Id: 1355
Gene Symbol: COX15
COX15
CUI: C0023264
Disease: Leigh Disease
Leigh Disease 		0.740 GeneticVariation UNIPROT Functional and genetic studies demonstrate that mutation in the COX15 gene can cause Leigh syndrome. 15235026

2004