mitochondrial oxidative phosphorylation disorder
Go to external page http://purl.obolibrary.org/obo/MONDO_0016387
Synonyms: OXPHOS disease OXPHOS system deficiency
This is just here as a test because I lose it
Term information
database
cross reference
- GARD:20546 (MONDO:GARD)
- Orphanet:223713 (MONDO:equivalentTo)
- MEDGEN:1825947 (MONDO:equivalentTo)
- UMLS:C5679825 (MONDO:equivalentTo)
- icd11.foundation:1204111545 (https://orcid.org/0000-0002-4142-7153)
Subsets
gard_rare, otar, disease_grouping, rare, ordo_group_of_disorders
exactMatch
http://identifiers.org/medgen/1825947
http://linkedlifedata.com/resource/umls/id/C5679825
http://www.orpha.net/ORDO/Orphanet_223713
Term relations
Equivalent to:
- inborn mitochondrial metabolism disorder and disease causes disruption of some oxidative phosphorylation