Disorder of glycosylation
MONDO:0024322A disease that has its basis in the disruption of glycosylation.
Also known as: disorder of glycosylation, glycosylation disease
74 clinical trials for this condition and its sub-types, 0 tagged with Disorder of glycosylation itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Disorder of glycosylation
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Disorder of GPI anchor biosynthesis 0 trials · 73 incl. sub-types
11 sub-types
- Paroxysmal nocturnal hemoglobinuria 73 trials Sub-types →
- Developmental and epileptic encephalopathy, 55 0 trials
- Developmental and epileptic encephalopathy, 77 0 trials
- Developmental and epileptic encephalopathy, 80 0 trials
- Glycosylphosphatidylinositol biosynthesis defect 15 0 trials
- Glycosylphosphatidylinositol biosynthesis defect 16 0 trials
- Glycosylphosphatidylinositol biosynthesis defect 17 0 trials
- Glycosylphosphatidylinositol biosynthesis defect 18 0 trials
- Glycosylphosphatidylinositol biosynthesis defect 25 0 trials
- Inborn disorder of glycosphingolipid and glycosylphosphatidylinositol anchor glycosylation 0 trials Sub-types →
- Neurodevelopmental disorder with hypotonia and cerebellar atrophy, with or without seizures 0 trials
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DHDDS-CDG 1 trial
1 sub-type
- Retinitis pigmentosa 59 0 trials
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Congenital myasthenic syndrome 12 0 trials
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Schneckenbecken dysplasia 0 trials
Most studied deeper sub-types
CHIME syndrome
(0)
GM3 synthase deficiency
(0)
Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
(0)
Hyperphosphatasia-intellectual disability syndrome
(0)
Hyperphosphatasia with intellectual disability syndrome 1
(0)
Hyperphosphatasia with intellectual disability syndrome 2
(0)
Hyperphosphatasia with intellectual disability syndrome 3
(0)
Hyperphosphatasia with intellectual disability syndrome 4
(0)
Hyperphosphatasia with intellectual disability syndrome 5
(0)
Hyperphosphatasia with intellectual disability syndrome 6
(0)
Intellectual disability, autosomal recessive 53
(0)
Multiple congenital anomalies-hypotonia-seizures syndrome 1
(0)
Multiple congenital anomalies-hypotonia-seizures syndrome 2
(0)
Multiple congenital anomalies-hypotonia-seizures syndrome 3
(0)
Paroxysmal nocturnal hemoglobinuria 1
(0)
Paroxysmal nocturnal hemoglobinuria 2
(0)
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