?combined oxidative phosphorylation deficiency 21 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/615918
Similar Terms
Downloads & Tools

Genes

1 genes associated with the ?combined oxidative phosphorylation deficiency 21 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
TARS2 threonyl-tRNA synthetase 2, mitochondrial (putative)