WT1

PanelMode of inheritanceDetails
7 panels
Signed-off version 2.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Familial Wilms tumor
Signed-off version 5.11
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Wagner Syndrome, Frasier syndrome, 136680, Nephrotic syndrome, type 4, 256370, Denys-Drash syndrome, 194080, Familial Wilms tumor, Wilms Tumor 1, Wilms Tumor, Wilms tumour, Meacham syndrome, 608978, Mesothelioma, somatic, 156240, Denys-Drash Syndrome, Wilms tumor, type 1, 194070
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 7.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
DENYS-DRASH SYNDROME 194080, FRASIER SYNDROME FRASIER SYNDROME FRASIER SYNDROME 136680
R-numbers: R146
Signed-off version 4.20
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Denys-Drash syndrome 194080, Frasier syndrome 136680, Meacham syndrome 608978
R-numbers: R456
Signed-off version 1.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Frasier syndrome, OMIM:136680, Wilms tumor, type 1, OMIM:194070, Wilms tumor 1, MONDO:0008679, Frasier syndrome, MONDO:0007635, Denys-Drash syndrome, OMIM:194080, Denys-Drash syndrome, MONDO:0008682
R-numbers: R21, R412
Signed-off version 7.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
FRASIER SYNDROME FRASIER SYNDROME FRASIER SYNDROME, DENYS-DRASH SYNDROME
Component of the following Super Panels:
  • - Unexplained young onset end-stage renal disease
R-numbers: R195
Signed-off version 6.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Denys-Drash syndrome #194080, Frasier syndrome #136680, Wilms tumor, type 1 #194070