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Kidney Tissue Atlas Ontology
Last uploaded:
March 16, 2024
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| Id | http://purl.obolibrary.org/obo/MONDO_0004069
http://purl.obolibrary.org/obo/MONDO_0004069
|
|---|---|
| Preferred Name | inborn mitochondrial metabolism disorder |
| 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.
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| Synonyms |
mitochondrial metabolism disease
mitochondrial genetic disorders
mitochondrial disease
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| label |
inborn mitochondrial metabolism disorder
|
|---|---|
| prefLabel |
inborn mitochondrial metabolism disorder
|
| exactMatch | |
| database_cross_reference |
Orphanet:68380
GARD:0007048
DOID:700
MESH:D028361
|
| notation |
MONDO:0004069
|
| in_subset | |
| has related synonym |
mitochondrial metabolism disease
mitochondrial genetic disorders
|
| id |
MONDO:0004069
|
| see also | |
| 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 | |
| imported from | |
| closeMatch | |
| type | |
| conformsTo | |
| has exact synonym |
mitochondrial disease
|
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