Disorder of GPI anchor biosynthesis
MONDO:0024321A disease that has its basis in the disruption of GPI anchor biosynthetic process.
Also known as: GPI anchor biosynthetic process disease, GPIBD, disorder of GPI anchor biosynthetic process, glycosylphosphatidylinositol biosynthesis defect
73 clinical trials for this condition and its sub-types, 0 tagged with Disorder of GPI anchor biosynthesis itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Disorder of GPI anchor biosynthesis
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Paroxysmal nocturnal hemoglobinuria 73 trials
2 sub-types
- Paroxysmal nocturnal hemoglobinuria 1 0 trials
- Paroxysmal nocturnal hemoglobinuria 2 0 trials
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8 sub-types
- CHIME syndrome 0 trials
- GM3 synthase deficiency 0 trials
- Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency 0 trials
- Hyperphosphatasia-intellectual disability syndrome 0 trials Sub-types →
- Intellectual disability, autosomal recessive 53 0 trials
- Multiple congenital anomalies-hypotonia-seizures syndrome 1 0 trials
- Multiple congenital anomalies-hypotonia-seizures syndrome 2 0 trials
- Multiple congenital anomalies-hypotonia-seizures syndrome 3 0 trials
Most studied deeper sub-types
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)
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