GGDonto: Genetic Glyco-Diseases Ontology
Legend:
Concept Types
target (multiple types disease)
classification term
pathway-based classification term
clinical findings
multiple types disease
single disease
disease type
'Mucopolysaccharidosis III'
Congenital, Hereditary, and Neonatal Diseases and Abnormalities related to Glycans
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Lysosomal Storage Diseases
(degradation)
Pathogenesis
Genetic disorders of glycan degradation
Disorders of glycosaminoglycan metabolism
Mucopolysaccharidosis III
Sanfilippo syndrome A
(GDGDB)
[SGSH]
Sanfilippo syndrome B
(GDGDB)
[NAGLU]
Sanfilippo syndrome C
(GDGDB)
[HGSNAT]
Sanfilippo syndrome D
(GDGDB)
[GNS]
Hereditary disorders by systems
Genetic disorders of glycan degradation (by systems, signs and symptoms)
Diseases
Cardiovascular Diseases
Heart Diseases
Heart Failure
Mucopolysaccharidosis III
Heart Valve Diseases
Mucopolysaccharidosis III
Myocardial Ischemia
Coronary Disease
Coronary Artery Disease
Mucopolysaccharidosis III
Vascular Diseases
Peripheral Vascular Diseases
Mucopolysaccharidosis III
Myocardial Ischemia
Coronary Disease
Coronary Artery Disease
Mucopolysaccharidosis III
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Mucinoses
Mucopolysaccharidosis III
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