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Carnitine palmitoyltransferase II deficiency

Disease Summary
Associated Targets (1)


Disease Ontology Description A lipid metabolism disorder characterized by an enzymatic defect that prevents long-chain fatty acids from being transported into the mitochondria.
DataSource References
eRAM: DOID:0060235
JensenLab Knowledge GHR: DOID:0060235
Target Novelty (Tin-x)