Preferred Name

inborn mitochondrial metabolism disorder
Synonyms

mitochondrial metabolism disease

mitochondrial genetic disorders

mitochondrial disease

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

relatedMatch

http://linkedlifedata.com/resource/umls/id/CN552492

seeAlso

https://rarediseases.info.nih.gov/diseases/7048/mitochondrial-genetic-disorders

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

http://purl.obolibrary.org/obo/MONDO_0015327

http://purl.obolibrary.org/obo/MONDO_0044970

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