|
cardiomyopathy, infantile hypertrophic mitochondrial, and lactic acidosis
|
13865 |
|
|
mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency
|
13865 |
|
|
combined oxidative phosphorylation defect type 10
|
13865 |
|
|
MTO1 combined oxidative phosphorylation deficiency
|
13865 |
|
|
combined oxidative phosphorylation deficiency 10
|
13865 |
|
|
combined oxidative phosphorylation deficiency 10; COXPD10
|
http://purl.obolibrary.org/obo/MONDO_0013865 |
|
|
combined oxidative phosphorylation deficiency caused by mutation in MTO1
|
13865 |
|
|
combined oxidative phosphorylation deficiency type 10
|
13865 |
|
