Search Ontology:
Human Disease
mitochondrial complex V (ATP synthase) deficiency
- Term ID
- DOID:0111143
- Synonyms
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- 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
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- GARD:1459
- ORDO:254913
- SNOMEDCT_US_2023_03_01:780820008
- UMLS_CUI:C4757950
- Ontology
- Human Disease ( DOID:0111143 )
- is a type of
-
- has subtype
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Genes Involved
Zebrafish Models