combined oxidative phosphorylation deficiency 11 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/614922
Similar Terms
Downloads & Tools

Genes

1 genes associated with the combined oxidative phosphorylation deficiency 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
RMND1 required for meiotic nuclear division 1 homolog (S. cerevisiae)