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
Genetic disorders of glycan synthesis
'Cardiomyopathy, dilated, 1X'
(
Integration tree
)
Pathogenesis (traditional nomenclature)
Genetic disorders of glycan synthesis (traditional nomenclature)
Disorders of O-linked glycosylation
Defects in O-mannose glycans
Cardiomyopathy, dilated, 1X
(GDGDB)
[FKTN]
Pathogenesis (new nomenclature)
Genetic disorders of glycan synthesis (new nomenclature)
Congenital disorders of glycosylation (CDGs)
Defects in protein O-glycosylation
Defects in O-mannosylglycan synthesis
FKTN-CDG (cong. muscular dystrophy spectrum)
Cardiomyopathy, dilated, 1X
(GDGDB)
[FKTN]
Genetic disorders of glycan synthesis (by systems, signs and symptoms)
Genetic disorders of glycan synthesis (by systems, signs and symptoms)
Diseases
Cardiovascular Diseases
Heart Diseases
Cardiomegaly
Cardiomyopathy, dilated, 1X
(GDGDB)
[FKTN]
Cardiomyopathies
Cardiomyopathy, dilated, 1X
(GDGDB)
[FKTN]
Cardiomyopathy, dilated, 1X
(GDGDB)
[FKTN]
Musculoskeletal Diseases
Muscular Diseases
Muscle Weakness
Cardiomyopathy, dilated, 1X
(GDGDB)
[FKTN]
Muscular Disorders, Atrophic
Muscular Dystrophies
Cardiomyopathy, dilated, 1X
(GDGDB)
[FKTN]
Nervous System Diseases
Neurologic Manifestations
Neuromuscular Manifestations
Muscle Hypotonia
Cardiomyopathy, dilated, 1X
(GDGDB)
[FKTN]
Muscular Atrophy
Cardiomyopathy, dilated, 1X
(GDGDB)
[FKTN]
Muscle Weakness
Cardiomyopathy, dilated, 1X
(GDGDB)
[FKTN]
Neuromuscular Diseases
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Cardiomyopathy, dilated, 1X
(GDGDB)
[FKTN]
Pathological Conditions, Signs and Symptoms
Signs and Symptoms
Mobility Limitation
Cardiomyopathy, dilated, 1X
(GDGDB)
[FKTN]
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