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Disease Congenital disorder of glycosylation type 1A

Name Congenital disorder of glycosylation type 1A
Synonyms Carbohydrate-deficient glycoprotein syndrome type 1A | Carbohydrate-Deficient Glycoprotein Syndrome Type Ia | CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME, TYPE Ia, FORMERLY | CDG1A | CDGIa | CDG Ia | Congenital Disorder of Glycosylation Type Ia | Congenital Disorder of Glycosylation, Type Ia | Jaeken syndrome | Phosphomannomutase 2 deficiency
Categories Genetic disease (inborn) | Metabolic disease
MeSH® ID C535739
OMIM® ID 212065

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 1A 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 1A Has associated chemicals Has associated genes

Top ↑ Descendants

None.