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
'Anemia, Hemolytic'
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
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Hemolytic
Hemoglobinuria, Paroxysmal
Paroxysmal nocturnal hemoglobinuria, somatic (SOMATIC MUTATION)
(GDGDB)
[PIGA]
Anemia, Hemolytic, Congenital
Anemia, Dyserythropoietic, Congenital
SEC23B-CDG
(GDGDB)
[SEC23B]
Anemia, Hemolytic, Autoimmune
Tn polyagglutination syndrome, somatic (SOMATIC MUTATION)
[C1GALT1C1]
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