ONKI3 | Medical Subject Headings

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The way property values are displayed: value/row values side by side

The way concept relations are shown: separately in hierarchy

Mitochondrial Diseases

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Mitochondrial Diseases 17 coordinate concepts 9 subordinate concepts ∟ Carbamoyl-Phosphate Synthase I Deficiency Disease \| ∟ Cytochrome-c Oxidase Deficiency \| ∟ Friedreich Ataxia \| ∟ Leigh Disease \| ∟ Mitochondrial Myopathies \| ∟ Optic Atrophy, Autosomal Dominant \| ∟ Optic Atrophy, Hereditary, Leber \| ∟ Pyruvate Carboxylase Deficiency Disease \| ∟ Pyruvate Dehydrogenase Complex Deficiency Disease ∟ Acid-Base Imbalance \| ∟ Amyloidosis \| ∟ Brain Diseases, Metabolic \| ∟ Calcium Metabolism Disorders \| ∟ D008659Q000151* \| ∟ DNA Repair-Deficiency Disorders \| ∟ Glucose Metabolism Disorders \| ∟ Iron Metabolism Disorders \| ∟ Lipid Metabolism Disorders \| ∟ Malabsorption Syndromes \| ∟ Metabolic Syndrome X \| ∟ Metabolism, Inborn Errors \| ∟ Phosphorus Metabolism Disorders \| ∟ Porphyrias \| ∟ Skin Diseases, Metabolic \| ∟ Wasting Syndrome \| ∟ Water-Electrolyte Imbalance X
Broader terms:	Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Mitochondrial Diseases Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) X
Narrower terms:	Carbamoyl-Phosphate Synthase I Deficiency Disease \| Cytochrome-c Oxidase Deficiency \| Friedreich Ataxia \| Leigh Disease \| Mitochondrial Myopathies \| Optic Atrophy, Autosomal Dominant \| Optic Atrophy, Hereditary, Leber \| Pyruvate Carboxylase Deficiency Disease \| Pyruvate Dehydrogenase Complex Deficiency Disease X
Annotation:	GEN or unspecified; prefer specifics X
History note:	Mitochondria (1987-2001) \| Mitochondrial Myopathies (1992-2001)X
historyNote*:	2002; use MITOCHONDRIAL MYOPATHIES 2000-2001 X
publicMeSHNote*:	2002; see MITOCHONDRIAL MYOPATHIES 2000-2001 X
Scope note:	Diseases caused by abnormal function of the MITOCHONDRIA. They may be caused by mutations, acquired or inherited, in mitochondrial DNA or in nuclear genes that code for mitochondrial components. They may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes. X
activeMeSHYear*:	2002 \| 2003 \| 2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	2001-08-03X
dateEstablished*:	2002-01-01X
recordAuthorizer*:	sjnX
recordMaintainer*:	jlsX
recordOriginator*:	nnsX
Type:	Concept X
Coordinate terms:	Acid-Base Imbalance \| Amyloidosis \| Brain Diseases, Metabolic \| Calcium Metabolism Disorders \| D008659Q000151* \| DNA Repair-Deficiency Disorders \| Glucose Metabolism Disorders \| Iron Metabolism Disorders \| Lipid Metabolism Disorders \| Malabsorption Syndromes \| Metabolic Syndrome X \| Metabolism, Inborn Errors \| Phosphorus Metabolism Disorders \| Porphyrias \| Skin Diseases, Metabolic \| Wasting Syndrome \| Water-Electrolyte Imbalance X
URI:	X
Labels and equivalent concepts:	Mitokondriotaudit (fi) Mitokondriosairaus (fi, replaced) Mitokondriotauti (fi, replaced) Mitokondriosairaudet (fi, replaced) Mitokondriella sjukdomar (sv) Mitochondrial Respiratory Chain Deficiencies (en, replaced) Mitochondrial Electron Transport Chain Deficiencies (en, replaced) Mitochondrial Disorders (en, replaced) X
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