mitochondrial complex iv deficiency Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_3762)
External Link http://www.omim.org/entry/220110
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Genes

5 genes associated with the mitochondrial complex iv deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
APOPT1 apoptogenic 1, mitochondrial
COA5 cytochrome c oxidase assembly factor 5
COX10 COX10 heme A:farnesyltransferase cytochrome c oxidase assembly factor
COX20 COX20 cytochrome c oxidase assembly factor
PET100 PET100 homolog (S. cerevisiae)