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
'Wolman disease'
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 sphingolipid metabolism and other lipid storage disorders
Other lipid storage disorders
Wolman disease
(GDGDB)
[LIPA]
Hereditary disorders by systems
Genetic disorders of glycan degradation (by systems, signs and symptoms)
Diseases
Digestive System Diseases
Liver Diseases
Hepatomegaly
Wolman disease
(GDGDB)
[LIPA]
Endocrine System Diseases
Adrenal Gland Diseases
Wolman disease
(GDGDB)
[LIPA]
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Wolman disease
(GDGDB)
[LIPA]
Lymphatic Diseases
Splenic Diseases
Wolman disease
(GDGDB)
[LIPA]
Nervous System Diseases
Neurologic Manifestations
Neuromuscular Manifestations
Muscle Hypotonia
Wolman disease
(GDGDB)
[LIPA]
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Growth Disorders
Wolman disease
(GDGDB)
[LIPA]
Hyperbilirubinemia
Jaundice
Wolman disease
(GDGDB)
[LIPA]
Signs and Symptoms
Signs and Symptoms, Digestive
Diarrhea
Wolman disease
(GDGDB)
[LIPA]
Vomiting
Wolman disease
(GDGDB)
[LIPA]
Psychiatry and Psychology
Mental Disorders
Mental Disorders Diagnosed in Childhood
Developmental Disabilities
Wolman disease
(GDGDB)
[LIPA]
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