mitochondrial disorder due to a defect in mitochondrial protein synthesis

Go to external page http://purl.obolibrary.org/obo/MONDO_0018157


This is just here as a test because I lose it

Term information

database cross reference
  • UMLS:CN227273 (MONDO:equivalentTo)
  • Orphanet:35696 (MONDO:equivalentTo)
  • ICD10:E88.8 (Orphanet:35696)
Subsets

ordo_group_of_disorders

abbreviation
COXPD [ Orphanet:35696 ]

exactMatch

http://linkedlifedata.com/resource/umls/id/CN227273

http://www.orpha.net/ORDO/Orphanet_35696

has exact synonym

COXPD

combined OXPHOS defect

combined oxidative phosphorylation defect

combined OXPHOS deficiency

id

MONDO:0018157