Experimental Factor Ontology

Last uploaded: November 18, 2024
Preferred Name

mitochondrial disease
Synonyms
ID

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

curated_content_resource

https://search.clinicalgenome.org/kb/conditions/MONDO:0044970

database_cross_reference

MEDGEN:155901

UMLS:C0751651

NANDO:2100163

NANDO:1200173

disease has basis in dysfunction of

http://purl.obolibrary.org/obo/GO_0005739

exactMatch

http://linkedlifedata.com/resource/umls/id/C0751651

http://identifiers.org/medgen/155901

id

MONDO:0044970

in taxon

http://purl.obolibrary.org/obo/NCBITaxon_9606

in_subset

http://purl.obolibrary.org/obo/mondo/mondo-base#clingen

http://purl.obolibrary.org/obo/mondo/mondo-base#otar

http://purl.obolibrary.org/obo/mondo/mondo-base#rare_grouping

label

mitochondrial disease

notation

MONDO:0044970

preferred label

mitochondrial disease

prefLabel

mitochondrial disease

see also

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

subClassOf

http://www.ebi.ac.uk/efo/EFO_0000408

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