Diseases of propionyl-CoA catabolism

Stable Identifier
R-HSA-9759785
Type
Pathway
Species
Homo sapiens
ReviewStatus
5/5
Locations in the PathwayBrowser
Expand all
General
SVG | 
PNG
Low
Medium
High
 | PPTX  | SBGN
Diseases of propionyl-CoA catabolism
Click the image above or here to open this pathway in the Pathway Browser
Propionyl-CoA catabolism is the aspect of mitochondrial beta-oxidation affected by the one disease of this process annotated in Reactome.
Literature References
PubMed ID Title Journal Year
16281286 Spectrum of mutations in mut methylmalonic acidemia and identification of a common Hispanic mutation and haplotype

Niles, K, Worgan, LC, Rosenblatt, DS, Lepage, P, Hofmann, A, Kucic, T, Tirone, JC, Sammak, A, Verner, A

Hum. Mutat. 2006
Participants
Events
Participates
as an event of
Disease
Name Identifier Synonyms
lipid metabolism disorder DOID:3146 dyslipidemia, fatty acid metabolism disorder
Authored
Jassal, B  (2013-05-13)
Reviewed
D'Eustachio, P  (2021-12-13)
Created
D'Eustachio, P  (2021-12-13)
Cite Us!