Search Ontology:
Human Disease

mitochondrial complex V (ATP synthase) deficiency

Term ID
DOID:0111143
Synonyms
Definition
A mitochondrial metabolism disease characterized by impaired function of one or more of the proteins making up the mitochondrial proton-transporting ATP synthase complex. https://www.ncbi.nlm.nih.gov/pubmed/21874297
References
  • GARD:1459
  • ORDO:254913
  • SNOMEDCT_US_2023_03_01:780820008
  • UMLS_CUI:C4757950
Ontology
Human Disease   ( DOID:0111143 )
Relationships
is a type of
has subtype
Other Pages
Genes Involved
Zebrafish Models