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
'CDG-IIf' 'SLC35A1-CDG'
Congenital, Hereditary, and Neonatal Diseases and Abnormalities related to Glycans
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
(synthesis)
Pathogenesis
Genetic disorders of glycan synthesis (traditional nomenclature)
Defects in N-glycan biosynthesis
Disorders of N-linked glycosylation - Congenital disorders of glycosylation (CDGs)
Type II CDGs
CDG-IIf
[SLC35A1]
Genetic disorders of glycan synthesis (new nomenclature)
Congenital disorders of glycosylation (CDGs)
Defects in multiple glycosylation and other pathways
Defects in nucleotide-sugar transport
SLC35A1-CDG
[SLC35A1]
Hereditary disorders by systems
Genetic disorders of glycan synthesis (by systems, signs and symptoms)
Diseases
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Platelet Disorders
Thrombocytopenia
SLC35A1-CDG
[SLC35A1]
Hemorrhagic Disorders
SLC35A1-CDG
[SLC35A1]
Leukocyte Disorders
Leukopenia
Agranulocytosis
Neutropenia
SLC35A1-CDG
[SLC35A1]
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Hemorrhage
SLC35A1-CDG
[SLC35A1]
Respiratory Tract Diseases
Respiratory Tract Infections
SLC35A1-CDG
[SLC35A1]
Immune System Diseases
Immunologic Deficiency Syndromes
SLC35A1-CDG
[SLC35A1]
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