PhenomeGene — Human Disease Gene Website SeriesPIGV

Families

Pathogenic germline mutations in PIGVlead to glycosylphosphatidylinositol biosynthesis deficiency (GPIBD). Individuals with pathogenic biallelic mutations in genes of the glycosylphosphatidylinositol (GPI)-anchor pathway exhibit cognitive impairments, motor delay, and often epilepsy.