mitochondrial disease - Ontology Report - Rat Genome Database

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EXPERIMENTAL FACTOR ONTOLOGY - ANNOTATIONS	{{ watchLinkText }}

Term:	mitochondrial disease	go back to main search page
Accession:	EFO:MONDO:0044970	browse the term
Synonyms:	alt_id:	MONDO:0044970
	xref:	MEDGEN:155901; NANDO:1200173; NANDO:2100163; UMLS:C0751651
	external_ontology:	disease_has_basis_in_dysfunction_of EFO:GO:0005739
	see_also:	https://www.epilepsydiagnosis.org/aetiology/metabolic-groupoverview.html#mitochondrial
	external_ontology:	in_taxon EFO:NCBITaxon:9606

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Term paths to the root

Path 1
Term	Annotations
experimental factor	0
material property	0
disposition	0
disease	0
mitochondrial disease	0
Bjornstad syndrome	0
GRACILE syndrome	0
X-linked sideroblastic anemia with ataxia	0
auditory neuropathy-optic atrophy syndrome	0
autosomal dominant optic atrophy plus syndrome +	0
ethylmalonic encephalopathy	0
hereditary myopathy with lactic acidosis due to ISCU deficiency	0
inborn mitochondrial metabolism disorder +	0
maternally-inherited cardiomyopathy and hearing loss	0
mitochondrial short-chain Enoyl-Coa hydratase 1 deficiency	0
optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome	0
pure mitochondrial myopathy	0

paths to the root