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
'Bruck syndrome 2'
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)
Disorders of O-linked glycosylation
Defects in O-galactosyl glycan biosynthesis
Bruck syndrome 2
(GDGDB)
[PLOD2]
Hereditary disorders by systems
Genetic disorders of glycan synthesis (by systems, signs and symptoms)
Diseases
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Osteochondrodysplasias
Osteogenesis Imperfecta
Bruck syndrome 2
(GDGDB)
[PLOD2]
Bone Diseases, Metabolic
Osteoporosis
Bruck syndrome 2
(GDGDB)
[PLOD2]
Joint Diseases
Contracture
Bruck syndrome 2
(GDGDB)
[PLOD2]
Bruck syndrome 2
(GDGDB)
[PLOD2]
Musculoskeletal Abnormalities
Limb Deformities, Congenital
Lower Extremity Deformities, Congenital
Foot Deformities, Congenital
Clubfoot
Bruck syndrome 2
(GDGDB)
[PLOD2]
Arthrogryposis
Bruck syndrome 2
(GDGDB)
[PLOD2]
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Hernia
Hernia, Abdominal
Hernia, Inguinal
Bruck syndrome 2
(GDGDB)
[PLOD2]
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Collagen Diseases
Osteogenesis Imperfecta
Bruck syndrome 2
(GDGDB)
[PLOD2]
Wounds and Injuries
Fractures, Bone
Fractures, Spontaneous
Bruck syndrome 2
(GDGDB)
[PLOD2]
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