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Multiple congenital anomalies-hypotonia-seizures syndrome 2

MONDO:0010466

Any multiple congenital anomalies/dysmorphic syndrome-intellectual disability in which the cause of the disease is a mutation in the PIGA gene.

Also known as: DEE20, GPIBD4, MCAHS type 2, MCAHS2, PIGA multiple congenital anomalies/dysmorphic syndrome-intellectual disability, developmental and epileptic encephalopathy 20, epileptic encephalopathy, early infantile, 20, glycosylphosphatidylinositol biosynthesis defect 4

17 clinical trials for this condition and its sub-types, 0 tagged with Multiple congenital anomalies-hypotonia-seizures syndrome 2 itself.

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