GGDonto: Genetic Glyco-Diseases Ontology
Legend:
Concept Types
target (clinical findings)
classification term
pathway-based classification term
clinical findings
multiple types disease
single disease
disease type
'Jaundice'
Congenital, Hereditary, and Neonatal Diseases and Abnormalities related to Glycans
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
(synthesis)
Hereditary disorders by systems
Genetic disorders of glycan synthesis (by systems, signs and symptoms)
Diseases
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Hyperbilirubinemia
Jaundice
DPAGT1-CDG
(GDGDB)
[DPAGT1]
COG7-CDG
(GDGDB)
[COG7]
SEC23B-CDG
(GDGDB)
[SEC23B]
Lysosomal Storage Diseases
(degradation)
Hereditary disorders by systems
Genetic disorders of glycan degradation (by systems, signs and symptoms)
Diseases
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Hyperbilirubinemia
Jaundice
Niemann-Pick disease, type A
(GDGDB)
[SMPD1]
Niemann-Pick disease, type C1
(GDGDB)
[NPC1]
Niemann-Pick disease, type C2
(GDGDB)
[NPC2]
Wolman disease
(GDGDB)
[LIPA]
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