mitochondrial complex v (atp synthase) deficiency, nuclear type 2 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A mitochondrial metabolism disease that has material basis in mutation in the TMEM70 gene on chromosome 8q21. (Human Disease Ontology, DOID_0060331)
External Link http://www.omim.org/entry/614052
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Genes

1 genes associated with the mitochondrial complex v (atp synthase) deficiency, nuclear type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
TMEM70 transmembrane protein 70