GGPS1

geranylgeranyl diphosphate synthase 1
OMIM: 606982
PanelMode of inheritanceDetails
2 panels
Component of the following Super Panels:
  • - Hypotonic infant
  • - Other rare neuromuscular disorders
R-numbers: R79
Signed-off version 5.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome, OMIM:619518
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R67
Signed-off version 4.57
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome, OMIM:619518