SPEG

SPEG complex locus
OMIM: 615950
PanelMode of inheritanceDetails
4 panels
Component of the following Super Panels:
  • - Hypotonic infant
  • - Other rare neuromuscular disorders
R-numbers: R81
Signed-off version 4.38
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Centronuclear myopathy 5, OMIM:615959
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.6
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
CENTRONUCLEAR MYOPATHY WITH DILATED CARDIOMYOPATHY 615959
R-numbers: R21, R412
Signed-off version 4.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
CENTRONUCLEAR MYOPATHY WITH DILATED CARDIOMYOPATHY
Component of the following Super Panels:
  • - Unexplained death in infancy and sudden unexplained death in childhood
R-numbers: R135
Signed-off version 5.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Dilated cardiomyopathy, MONDO:0005021, Centronuclear myopathy 5, OMIM:615959