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Disease Carnitine palmitoyl transferase 2 deficiency

Name Carnitine palmitoyl transferase 2 deficiency
Synonyms Carnitine Palmitoyltransferase 2 Deficiency | Carnitine palmitoyltransferase deficiency type 2 | Carnitine Palmitoyltransferase Ii Deficiency | Cpt2 Deficiency | Cpt Ii Deficiency | Muscle form of carnitine palmitoyltransferase deficiency
Categories Genetic disease (inborn) | Metabolic disease
MeSH® ID C535589
External Links

Top ↑ Ancestors

1. DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities Has associated chemicals Has associated genes Has associated exposure references Genetic Diseases, Inborn Has associated chemicals Has associated genes Has associated exposure references Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated exposure references Carnitine palmitoyl transferase 2 deficiency
2. DiseasesNutritional and Metabolic Diseases Has associated chemicals Has associated genes Has associated exposure references Metabolic Diseases Has associated chemicals Has associated genes Has associated exposure references Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated exposure references Carnitine palmitoyl transferase 2 deficiency

Top ↑ Descendants

None.