Table 5.

Clinically relevant annotations enriched with Cluster 1 genes.

GO ID	GO Term	Adjusted p-value∗	Associated genes found
C0751651	Mitochondrial diseases	7.8E-14	NDUFA10, NDUFA12, NDUFA2, NDUFA9, NDUFB9, NDUFS1, NDUFS4, NDUFS6, NDUFS8, NDUFV1, NDUFV2
C1838979	Mitochondrial complex I deficiency	4.6E-10	NDUFB9, NDUFS1, NDUFS4, NDUFS6, NDUFV1, NDUFV2
C0236038	Hereditary hearing loss and deafness	5.1E-10	NDUFA10, NDUFA12, NDUFA2, NDUFA9, NDUFB9, NDUFS1, NDUFS4, NDUFS6, NDUFS8, NDUFV1, NDUFV2
C0023264	Leigh syndrome	5.6E-10	NDUFA10, NDUFA12, NDUFA2, NDUFA9, NDUFS4, NDUFS8

^∗The raw p-values were adjusted using the Bonferroni step down method.