PIGT-CDG

Synonym(s)
- Multiple congenital anomalies-hypotonia-seizures syndrome type 3, GPI biosynthesis defect type 7
Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- PIGT / Phosphatidylinositol Glycan Anchor Biosynthesis Class T
  20q13.12
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Phosphatidylinositol glycan anchor biosynthesis class T protein
Disease group(s)
- 18.3.1 Disorders of glycosylphosphatidylinositol biosynthesis