| Disease Browser
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Parent Node:
 Kearns-Sayre Syndrome (D007625) | Parent Node:
Mitochondrial Myopathies (D017240) | ..Starting node
.. Mitochondrial cytopathy (C540770)
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Child Nodes:
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Sister Nodes: | ..Combined Oxidative Phosphorylation Deficiency 3 (C566467)
| ..Mitochondrial cytopathy (C540770)
| ..MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE) (OMIM:609560)
| ..Mitochondrial Dna Depletion Syndrome, Encephalomyopathic Form, With Methylmalonic Aciduria, Autosomal Recessive (C567624)
| ..Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form, Autosomal Recessive (C567608)
| ..Mitochondrial Encephalomyopathies (D017237)  13
| ..Mitochondrial Myopathy with a Defect in Mitochondrial Protein Transport (C565376)
| ..Mitochondrial Myopathy with Diabetes (C564026)
| ..Mitochondrial myopathy with lactic acidosis (C537476)
| ..Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay (C567769)
| ..Myopathy, Mitochondrial, Lethal Infantile (C564017)
| ..Neuropathy ataxia and retinis pigmentosa (C537396)
| ..Ophthalmoplegia, Chronic Progressive External (D017246) 7
| ..Trifunctional Protein Deficiency With Myopathy And Neuropathy (C566945)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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| Term ID: | 7310 |
| Name: | Mitochondrial cytopathy |
| Definition: | |
| Alternative IDs: | |
| ParentIDs: | MESH:D007625|MESH:D017240 |
| TreeNumbers: | C05.651.460.700.500/C540770 |C05.651.460/C540770 |C10.292.562.775.500/C540770 |C10.668.491.500.700.500/C540770 |C10.668.491.500/C540770 |C11.590.641.500/C540770 |C11.768.585.658.500.627/C540770 |C14.280.238.510/C540770 |C18.452.660.410/C540770 |C18.452.660.560.70 |
| Synonyms: | |
| Slim Mappings: | Cardiovascular disease|Eye disease|Metabolic disease|Musculoskeletal disease|Nervous system disease |
| Reference: |
MedGen: C540770
MeSH: C540770
OMIM:
Genes: | | Phenotypes | | | Disease Causing ClinVar Variants | |
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