D018981Level 6
Congenital Disorders of Glycosylation
**Definition:** A genetically heterogeneous group of heritable disorders resulting from defects in protein N-glycosylation.
**Tree numbers:** - C16.320.565.202.125 - C18.452.648.202.125
**Synonyms:** - Carbohydrate-Deficient Glycoprotein Syndrome - Glycoprotein Syndrome, Carbohydrate-Deficient
GET
/api/v1/systems/mesh/nodes/D018981Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.