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
'Krabbe disease, late-onset 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
Krabbe disease
(GDGDB)
[GALC]
Krabbe disease, late-onset form
[GALC]
Hereditary disorders by systems
Genetic disorders of glycan degradation (by systems, signs and symptoms)
Diseases
Musculoskeletal Diseases
Muscular Diseases
Muscle Rigidity
Krabbe disease
(GDGDB)
[GALC]
Krabbe disease, late-onset form
[GALC]
Muscle Weakness
Krabbe disease
(GDGDB)
[GALC]
Krabbe disease, late-onset form
[GALC]
Nervous System Diseases
Neurologic Manifestations
Neuromuscular Manifestations
Muscle Hypertonia
Muscle Rigidity
Krabbe disease
(GDGDB)
[GALC]
Krabbe disease, late-onset form
[GALC]
Muscle Weakness
Krabbe disease
(GDGDB)
[GALC]
Krabbe disease, late-onset form
[GALC]
Seizures
Krabbe disease
(GDGDB)
[GALC]
Krabbe disease, late-onset form
[GALC]
Sensation Disorders
Hearing Disorders
Hearing Loss
Krabbe disease
(GDGDB)
[GALC]
Krabbe disease, late-onset form
[GALC]
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