PIGM

phosphatidylinositol glycan anchor biosynthesis class M
OMIM: 610273
PanelMode of inheritanceDetails
3 panels
Component of the following Super Panels:
  • - Hereditary ataxia and cerebellar anomalies, childhood onset
Signed-off version 8.7
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Glycosylphosphatidylinositol deficiency, OMIM:610293
Component of the following Super Panels:
  • - Paediatric disorders
  • - Unexplained death in infancy and sudden unexplained death in childhood
Signed-off version 9.56
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Glycosylphosphatidylinositol deficiency, OMIM:610293
Component of the following Super Panels:
  • - Hypotonic infant
  • - Leukodystrophy, childhood onset
  • - Paediatric disorders
  • - Unexplained death in infancy and sudden unexplained death in childhood
R-numbers: R98
Signed-off version 9.29
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Glycosylphosphatidylinositol deficiency, OMIM:610293