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Inborn disorder of glycosphingolipid and glycosylphosphatidylinositol anchor glycosylation

MONDO:0017748

Also known as: disorder of glycosphingolipid and GPI-anchored proteins glycosylation, disorder of glycosphingolipid and glycosylphosphatidylinositol anchor glycosylation

36 clinical trials for this condition and its sub-types.

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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)

Broader categories

Disease (618) Metabolic disease (215) Hereditary disease (172) Inherited lipid metabolism disorder (165) Inborn errors of metabolism (42) Human disease (14) Congenital disorder of glycosylation (6) Disease of genetic or genomic mechanism (2) Disease by developmental or physiological process (0) Disease by etiologic mechanism (0)

Trials to join now! 16 Not yet recruiting 4 Not yet finished but already full! 3 Completed 13