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
'Gaucher disease, type I'
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
Sphingolipidosis
Other sphingolipidosis
Gaucher disease
Gaucher disease, type I
(GDGDB)
[GBA]
Hereditary disorders by systems
Genetic disorders of glycan degradation (by systems, signs and symptoms)
Diseases
Digestive System Diseases
Liver Diseases
Hepatomegaly
Gaucher disease, type I
(GDGDB)
[GBA]
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Gaucher disease, type I
(GDGDB)
[GBA]
Blood Platelet Disorders
Thrombocytopenia
Gaucher disease, type I
(GDGDB)
[GBA]
Hemorrhagic Disorders
Gaucher disease, type I
(GDGDB)
[GBA]
Lymphatic Diseases
Splenic Diseases
Gaucher disease, type I
(GDGDB)
[GBA]
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Metabolic
Osteoporosis
Gaucher disease, type I
(GDGDB)
[GBA]
Joint Diseases
Arthritis
Gaucher disease, type I
(GDGDB)
[GBA]
Musculoskeletal Abnormalities
Gaucher disease, type I
(GDGDB)
[GBA]
Nervous System Diseases
Neurologic Manifestations
Pain
Musculoskeletal Pain
Gaucher disease, type I
(GDGDB)
[GBA]
Respiratory Tract Diseases
Lung Diseases
Gaucher disease, type I
(GDGDB)
[GBA]
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