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Disease Congenital disorder of glycosylation type 1B

Name Congenital disorder of glycosylation type 1B
Synonyms Carbohydrate-deficient glycoprotein syndrome type 1B | CDG1B | CDG, GASTROINTESTINAL TYPE | CDGIb | CDG Ib | CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ib | Mannosephosphate isomerase deficiency | MPI DEFICIENCY | Protein-losing enteropathy-hepatic fibrosis syndrome | Saguenay-Lac Saint-Jean syndrome | SLSJ SYNDROME
Categories Genetic disease (inborn) | Metabolic disease
MeSH® ID C535740
OMIM® ID 602579

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 Congenital Disorders of Glycosylation Has associated chemicals Has associated genes Congenital disorder of glycosylation type 1B 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 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 1B Has associated chemicals Has associated genes

Top ↑ Descendants

None.