|
mitochondrial myopathy, infantile, transient; MMIT
|
http://purl.obolibrary.org/obo/MONDO_0010780 |
|
|
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 |
|
|
noninsulin-dependent diabetes mellitus with deafness
|
10785 |
|
|
Cox deficiency myopathy, infantile, transient
|
10780 |
|
|
Leber Hereditary optic atrophy
|
10788 |
|
|
Leber hereditary optic neuropathy
|
10788 |
|
|
Leber's hereditary optic neuropathy
|
10788 |
|
|
ataxia and polyneuropathy, adult-onset
|
10781 |
|
|
reversible infantile respiratory chain deficiency
|
10780 |
|
|
syndrome, actinic reticuloid
|
D010787 |
|
|
syndromes, actinic reticuloid
|
D010787 |
|
