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Up to: Developmental anomaly of metabolic origin · Inborn disorder of glycosphingolipid and glycosylphosphatidylinositol anchor glycosylation · Multiple congenital anomalies-hypotonia-seizures syndrome
Multiple congenital anomalies-hypotonia-seizures syndrome 1
Any multiple congenital anomalies/dysmorphic syndrome-intellectual disability in which the cause of the disease is a mutation in the PIGN gene.
This condition has no sub-types.