WT1

PanelMode of inheritanceDetails
7 panels
Signed-off version 2.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Familial Wilms tumor
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 2.2
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 2.2
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Denys-Drash syndrome 194080, Frasier syndrome 136680, Meacham syndrome 608978
R-numbers: R21
Signed-off version 1.92
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
FRASIER SYNDROME FRASIER SYNDROME FRASIER SYNDROME, DENYS-DRASH SYNDROME
R-numbers: R195
Signed-off version 2.32
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Denys-Drash syndrome #194080, Frasier syndrome #136680, Wilms tumor, type 1 #194070
R-numbers: R359
Signed-off version 2.5
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
R-numbers: R257
Signed-off version 1.2
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Nephrotic syndrome, type 4 256370