| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Mitochondrial-lipid-glycogen storage myopathy |
Is a |
True |
Mitochondrial myopathy |
Inferred relationship |
Some |
|
| Juvenile myopathy AND lactate acidosis |
Is a |
True |
Mitochondrial myopathy |
Inferred relationship |
Some |
|
| Fukuhara syndrome |
Is a |
False |
Mitochondrial myopathy |
Inferred relationship |
Some |
|
| Mitochondrial encephalomyopathy (disorder) |
Is a |
True |
Mitochondrial myopathy |
Inferred relationship |
Some |
|
| Maternally inherited mitochondrial cardiomyopathy and myopathy |
Is a |
True |
Mitochondrial myopathy |
Inferred relationship |
Some |
|
| Mitochondrial encephalocardiomyopathy due to transmembrane protein 70 mutation (disorder) |
Is a |
True |
Mitochondrial myopathy |
Inferred relationship |
Some |
|
| Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome (disorder) |
Is a |
True |
Mitochondrial myopathy |
Inferred relationship |
Some |
|
| Mitochondrial myopathy with sideroblastic anemia syndrome (disorder) |
Is a |
True |
Mitochondrial myopathy |
Inferred relationship |
Some |
|
| Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy (disorder) |
Is a |
True |
Mitochondrial myopathy |
Inferred relationship |
Some |
|
| Pure mitochondrial myopathy (disorder) |
Is a |
True |
Mitochondrial myopathy |
Inferred relationship |
Some |
|
| Mitochondrial myopathy, lactic acidosis, deafness syndrome |
Is a |
True |
Mitochondrial myopathy |
Inferred relationship |
Some |
|
| Adult-onset multiple mitochondrial deoxyribonucleic acid deletion syndrome due to deoxyguanosine kinase deficiency |
Is a |
True |
Mitochondrial myopathy |
Inferred relationship |
Some |
|
| Progressive external ophthalmoplegia, myopathy, emaciation syndrome |
Is a |
True |
Mitochondrial myopathy |
Inferred relationship |
Some |
|
| Lethal infantile mitochondrial myopathy (disorder) |
Is a |
True |
Mitochondrial myopathy |
Inferred relationship |
Some |
|
| Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial deoxyribonucleic acid mutation (disorder) |
Is a |
True |
Mitochondrial myopathy |
Inferred relationship |
Some |
|
| Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome |
Is a |
True |
Mitochondrial myopathy |
Inferred relationship |
Some |
|
| Childhood-onset spasticity with hyperglycinemia (disorder) |
Is a |
True |
Mitochondrial myopathy |
Inferred relationship |
Some |
|
| Periodic paralysis with later-onset distal motor neuropathy (disorder) |
Is a |
True |
Mitochondrial myopathy |
Inferred relationship |
Some |
|
| DNA2-related mitochondrial DNA deletion syndrome |
Is a |
True |
Mitochondrial myopathy |
Inferred relationship |
Some |
|
| Myopathy and diabetes mellitus (disorder) |
Is a |
True |
Mitochondrial myopathy |
Inferred relationship |
Some |
|
| Mitochondrial myopathy with reversible cytochrome C oxidase deficiency (disorder) |
Is a |
True |
Mitochondrial myopathy |
Inferred relationship |
Some |
|
| Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency |
Is a |
True |
Mitochondrial myopathy |
Inferred relationship |
Some |
|
| Maternally inherited mitochondrial myopathy (disorder) |
Is a |
True |
Mitochondrial myopathy |
Inferred relationship |
Some |
|
| Maternally inherited mitochondrial cardiomyopathy (disorder) |
Is a |
True |
Mitochondrial myopathy |
Inferred relationship |
Some |
|
| Autosomal dominant mitochondrial myopathy with exercise intolerance |
Is a |
True |
Mitochondrial myopathy |
Inferred relationship |
Some |
|
| Mitochondrial deoxyribonucleic acid depletion syndrome myopathic form (disorder) |
Is a |
True |
Mitochondrial myopathy |
Inferred relationship |
Some |
|
| Mitochondrial myopathy, cerebellar ataxia, pigmentary retinopathy syndrome |
Is a |
True |
Mitochondrial myopathy |
Inferred relationship |
Some |
|
| Combined oxidative phosphorylation defect type 39 |
Is a |
True |
Mitochondrial myopathy |
Inferred relationship |
Some |
|