GGDonto: Genetic Glyco-Diseases Ontology
Legend:
Concept Types
target (disease type)
classification term
pathway-based classification term
clinical findings
multiple types disease
single disease
disease type
'Gaucher disease, type II, perinatal lethal form'
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 II
(GDGDB)
[GBA]
Gaucher disease, type II, perinatal lethal form
[GBA]
Hereditary disorders by systems
Genetic disorders of glycan degradation (by systems, signs and symptoms)
Diseases
Musculoskeletal Diseases
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Maxillofacial Abnormalities
Gaucher disease, type II
(GDGDB)
[GBA]
Gaucher disease, type II, perinatal lethal form
[GBA]
Pathological Conditions, Signs and Symptoms
Signs and Symptoms
Edema
Hydrops Fetalis
Gaucher disease, type II
(GDGDB)
[GBA]
Gaucher disease, type II, perinatal lethal form
[GBA]
Skin and Connective Tissue Diseases
Skin Diseases
Skin Abnormalities
Ichthyosis
Gaucher disease, type II
(GDGDB)
[GBA]
Gaucher disease, type II, perinatal lethal form
[GBA]
Gaucher disease, type II
(GDGDB)
[GBA]
Gaucher disease, type II, perinatal lethal form
[GBA]
Stomatognathic Diseases
Stomatognathic System Abnormalities
Maxillofacial Abnormalities
Gaucher disease, type II
(GDGDB)
[GBA]
Gaucher disease, type II, perinatal lethal form
[GBA]
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