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Disease Cirrhosis, familial, with deposition of abnormal glycogen

Name Cirrhosis, familial, with deposition of abnormal glycogen
Categories Genetic disease (inborn) | Metabolic disease
MeSH® ID C537275

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 Carbohydrate Metabolism, Inborn Errors Has associated chemicals Has associated genes Glycogen Storage Disease Has associated chemicals Has associated genes Glycogen Storage Disease Type IV Has associated chemicals Has associated genes Cirrhosis, familial, with deposition of abnormal glycogen
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 Carbohydrate Metabolism, Inborn Errors Has associated chemicals Has associated genes Glycogen Storage Disease Has associated chemicals Has associated genes Glycogen Storage Disease Type IV Has associated chemicals Has associated genes Cirrhosis, familial, with deposition of abnormal glycogen

Top ↑ Descendants

None.