Skip navigation

Disease Carnitine-Acylcarnitine Translocase Deficiency

Name Carnitine-Acylcarnitine Translocase Deficiency
Synonyms CACTD | CACT Deficiency | Carnitine-Acylcarnitine Carrier Deficiency | Carnitine Acylcarnitine Translocase Deficiency
Categories Genetic disease (inborn) | Metabolic disease
MeSH® ID C562812
OMIM® ID 212138

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 Lipid Metabolism, Inborn Errors Has associated chemicals Has associated genes Carnitine-Acylcarnitine Translocase Deficiency Has associated chemicals Has associated genes
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 Lipid Metabolism Disorders Has associated chemicals Has associated genes Has associated exposure references Lipid Metabolism, Inborn Errors Has associated chemicals Has associated genes Carnitine-Acylcarnitine Translocase Deficiency Has associated chemicals Has associated genes
3. 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 Lipid Metabolism, Inborn Errors Has associated chemicals Has associated genes Carnitine-Acylcarnitine Translocase Deficiency Has associated chemicals Has associated genes

Top ↑ Descendants

None.