Diseases of propionyl-CoA catabolism

Stable Identifier
R-HSA-9759785
Type
Pathway
Species
Homo sapiens
ReviewStatus
5/5
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Diseases of propionyl-CoA catabolism
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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

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

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