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Disease Congenital disorder of glycosylation type 1X

Name Congenital disorder of glycosylation type 1X
Categories Blood disease | Genetic disease (inborn) | Metabolic disease
MeSH® ID C535751

Top ↑ Ancestors

1. DiseasesHemic and Lymphatic Diseases Has associated chemicals Has associated genes Has associated exposure references Hematologic Diseases Has associated chemicals Has associated genes Has associated exposure references Blood Platelet Disorders Has associated chemicals Has associated genes Has associated exposure references Thrombocytopenia Has associated chemicals Has associated genes Has associated exposure references Congenital disorder of glycosylation type 1X
2. 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 Congenital Disorders of Glycosylation Has associated chemicals Has associated genes Congenital disorder of glycosylation type 1X
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 Carbohydrate Metabolism, Inborn Errors Has associated chemicals Has associated genes Congenital Disorders of Glycosylation Has associated chemicals Has associated genes Congenital disorder of glycosylation type 1X

Top ↑ Descendants

None.