|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A mitochondrial metabolism disease that has material basis in mutation in the TMEM70 gene on chromosome 8q21. (Human Disease Ontology, DOID_0060331)|
|Downloads & Tools|
1 genes associated with the mitochondrial complex v (atp synthase) deficiency, nuclear type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
|TMEM70||transmembrane protein 70|