GGDonto: Genetic Glyco-Diseases Ontology
Legend:
Concept Types
target (single disease)
classification term
pathway-based classification term
clinical findings
multiple types disease
single disease
disease type
'DPM3-CDG'
Congenital, Hereditary, and Neonatal Diseases and Abnormalities related to Glycans
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
(synthesis)
Pathogenesis
Genetic disorders of glycan synthesis (new nomenclature)
Congenital disorders of glycosylation (CDGs)
Defects in protein N-glycosylation
Defects in lipid-linked oligosaccharide biosynthesis
DPM3-CDG
[DPM3]
Hereditary disorders by systems
Genetic disorders of glycan synthesis (by systems, signs and symptoms)
Diseases
Cardiovascular Diseases
Heart Diseases
Cardiomyopathies
DPM3-CDG
[DPM3]
DPM3-CDG
[DPM3]
Vascular Diseases
Cerebrovascular Disorders
DPM3-CDG
[DPM3]
Musculoskeletal Diseases
Muscular Diseases
Muscle Weakness
DPM3-CDG
[DPM3]
DPM3-CDG
[DPM3]
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Cerebrovascular Disorders
DPM3-CDG
[DPM3]
Neurologic Manifestations
Neuromuscular Manifestations
Muscular Atrophy
DPM3-CDG
[DPM3]
Muscle Weakness
DPM3-CDG
[DPM3]
Pathological Conditions, Signs and Symptoms
Signs and Symptoms
Mobility Limitation
DPM3-CDG
[DPM3]
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