FOXG1

PanelMode of inheritanceDetails
6 panels
R-numbers: R57
Signed-off version 3.56
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Rett Syndrome, congenital variant OMIM:613454, Rett syndrome, congenital variant MONDO:0013270
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 3.79
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
CONGENITAL VARIANT OF RETT SYNDROME 613454
Component of the following Super Panels:
  • - Paediatric disorders
  • - Unexplained death in infancy and sudden unexplained death in childhood
R-numbers: R59
Signed-off version 4.134
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Rett syndrome, congenital variantRett Syndrome, congenital variant OMIM:613454, Rett syndrome, congenital variant MONDO:0013270
R-numbers: R21, R412
Signed-off version 3.122
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Rett Syndrome, congenital variant OMIM:613454, Rett syndrome, congenital variant MONDO:0013270
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 5.343
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Rett Syndrome, congenital variant OMIM:613454, Rett syndrome, congenital variant MONDO:0013270
R-numbers: R88
Signed-off version 4.41
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Rett Syndrome, congenital variant OMIM:613454, Rett syndrome, congenital variant MONDO:0013270