Preferred Name | inborn mitochondrial metabolism disorder | |
Synonyms |
mitochondrial metabolism disease mitochondrial genetic disorders mitochondrial disease |
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Definitions |
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. |
|
ID |
http://purl.obolibrary.org/obo/MONDO_0004069 |
|
altLabel |
mitochondrial metabolism disease mitochondrial genetic disorders mitochondrial disease |
|
definition |
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. |
|
has_broad_synonym |
mitochondrial disease |
|
has_related_synonym |
mitochondrial metabolism disease mitochondrial genetic disorders |
|
label |
inborn mitochondrial metabolism disorder |
|
prefixIRI |
MONDO:0004069 |
|
prefLabel |
inborn mitochondrial metabolism disorder |
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relatedMatch | ||
seeAlso |
https://rarediseases.info.nih.gov/diseases/7048/mitochondrial-genetic-disorders |
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textual definition |
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. |
|
subClassOf |
http://purl.obolibrary.org/obo/MONDO_0019243 |