|
reversible infantile cytochrome C oxidase deficiency
|
10780 |
|
|
infantile reversible cytochrome C oxidase deficiency myopathy
|
10780 |
|
|
respiratory chain deficiency, infantile, transient
|
10780 |
|
|
maternally inherited diabetes and deafness
|
10785 |
|
|
diabetes and deafness, maternally inherited
|
10785 |
|
|
diabetes and deafness, maternally inherited; MIDD
|
http://purl.obolibrary.org/obo/MONDO_0010785 |
|
|
mitochondrial myopathy, infantile, transient
|
10780 |
|
|
chronic progressive external ophthalmoplegia with myopathy
|
10787 |
|
|
ophthalmoplegia, progressive external, with ragged red fibers
|
10787 |
|
|
ophthalmoplegia, progressive external, with ragged-Red fibers
|
10787 |
|
|
mitochondrial encephalomyopathy, lactic acidosis and stroke
|
10789 |
|
|
mitochondrial encephalomyopathy lactic acidosis and stroke-like episodes
|
10789 |
|
|
mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes
|
10789 |
|
|
mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes
|
10789 |
|
