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
Genetic disorders of glycan synthesis
'Optic Atrophies, Hereditary'
(
Integration tree
)
Pathogenesis (traditional nomenclature)
Genetic disorders of glycan synthesis (traditional nomenclature)
Pathogenesis (new nomenclature)
Genetic disorders of glycan synthesis (new nomenclature)
Genetic disorders of glycan synthesis (by systems, signs and symptoms)
Genetic disorders of glycan synthesis (by systems, signs and symptoms)
Diseases
Eye Diseases
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
ALG3-CDG
(GDGDB)
[ALG3]
POMT1/POMT2-CDG (cong. muscular dystrophy spectrum)
(GDGDB)
[POMT1,POMT2]
POMGNT1-CDG (cong. muscular dystrophy spectrum)
(GDGDB)
[POMGNT1]
Fukuyama congenital muscular dystrophy
(GDGDB)
[FKTN]
ST3GAL5-CDG
[SIAT9]
SRD5A3-CDG
[SRD5A3]
ALG13-CDG
[ALG13]
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
ALG3-CDG
(GDGDB)
[ALG3]
POMT1/POMT2-CDG (cong. muscular dystrophy spectrum)
(GDGDB)
[POMT1,POMT2]
POMGNT1-CDG (cong. muscular dystrophy spectrum)
(GDGDB)
[POMGNT1]
Fukuyama congenital muscular dystrophy
(GDGDB)
[FKTN]
ST3GAL5-CDG
[SIAT9]
SRD5A3-CDG
[SRD5A3]
ALG13-CDG
[ALG13]
Nervous System Diseases
Cranial Nerve Diseases
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
ALG3-CDG
(GDGDB)
[ALG3]
POMT1/POMT2-CDG (cong. muscular dystrophy spectrum)
(GDGDB)
[POMT1,POMT2]
POMGNT1-CDG (cong. muscular dystrophy spectrum)
(GDGDB)
[POMGNT1]
Fukuyama congenital muscular dystrophy
(GDGDB)
[FKTN]
ST3GAL5-CDG
[SIAT9]
SRD5A3-CDG
[SRD5A3]
ALG13-CDG
[ALG13]
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