Inborn disorder of glycosphingolipid and glycosylphosphatidylinositol anchor glycosylation
MONDO:0017748Also known as: disorder of glycosphingolipid and GPI-anchored proteins glycosylation, disorder of glycosphingolipid and glycosylphosphatidylinositol anchor glycosylation
0 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
CHIME syndrome
(0)
GM3 synthase deficiency
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Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
(0)
Hyperphosphatasia-intellectual disability syndrome
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Hyperphosphatasia with intellectual disability syndrome 1
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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
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Hyperphosphatasia with intellectual disability syndrome 6
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Intellectual disability, autosomal recessive 53
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Multiple congenital anomalies-hypotonia-seizures syndrome 1
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Multiple congenital anomalies-hypotonia-seizures syndrome 2
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Multiple congenital anomalies-hypotonia-seizures syndrome 3
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Broader categories
Disease
(680)
Metabolic disease
(233)
Inherited lipid metabolism disorder
(189)
Hereditary disease
(176)
Inborn errors of metabolism
(45)
Human disease
(14)
Congenital disorder of glycosylation
(7)
Disease of genetic or genomic mechanism
(2)
Disease by developmental or physiological process
(0)
Disease by etiologic mechanism
(0)
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