This is just here as a test because I lose it

Term information

id

MONDO:0044970

imported from

http://purl.obolibrary.org/obo/mondo.owl

oboInOwl:hasDefinition

Mitochondrial diseases (MIDs) are a large group of heterogeneous disorders due to mutations in either mitochondrial DNA (mtDNA) or nuclear DNA (nDNA) genes, the latter encoding proteins involved in mitochondrial function.

seeAlso

https://www.epilepsydiagnosis.org/aetiology/metabolic-groupoverview.html#mitochondrial

Term relations

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