GGDonto: Genetic Glyco-Diseases Ontology
Legend:
Concept Types
target (clinical findings)
classification term
pathway-based classification term
clinical findings
multiple types disease
single disease
disease type
'Cerebrovascular Disorders'
Congenital, Hereditary, and Neonatal Diseases and Abnormalities related to Glycans
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
(synthesis)
Hereditary disorders by systems
Genetic disorders of glycan synthesis (by systems, signs and symptoms)
Diseases
Cardiovascular Diseases
Vascular Diseases
Cerebrovascular Disorders
PMM2-CDG
(GDGDB)
[PMM2]
PMM2-CDG, infantile multisystem stage
[PMM2]
PMM2-CDG, late-infantile and childhood ataxia-intellectual disability stage
[PMM2]
PMM2-CDG, adult stable disability stage
[PMM2]
DPM3-CDG
[DPM3]
PGM1-CDG
[PGM1]
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Cerebrovascular Disorders
PMM2-CDG
(GDGDB)
[PMM2]
PMM2-CDG, infantile multisystem stage
[PMM2]
PMM2-CDG, late-infantile and childhood ataxia-intellectual disability stage
[PMM2]
PMM2-CDG, adult stable disability stage
[PMM2]
DPM3-CDG
[DPM3]
PGM1-CDG
[PGM1]
Lysosomal Storage Diseases
(degradation)
Hereditary disorders by systems
Genetic disorders of glycan degradation (by systems, signs and symptoms)
Diseases
Cardiovascular Diseases
Vascular Diseases
Cerebrovascular Disorders
Stroke
Fabry disease
(GDGDB)
[GLA]
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Cerebrovascular Disorders
Stroke
Fabry disease
(GDGDB)
[GLA]
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