Wilms Tumor, Aniridia, Genitourinary Anomalies, and Impaired Intellectual Development Syndrome (WAGR)

Alias:

Wagr Syndrome

11p Partial Monosomy Syndrome

Deletion 11p13

Wilms Tumor, Aniridia, Genitourinary Anomalies, and Mental Retardation Syndrome

Wilms Tumor-Aniridia-Genitourinary Anomalies-Intellectual Disability Syndrome

Chromosome 11p13 Deletion Syndrome

Monosomy 11p13

Del(11)(p13)

Wilms Tumor, Aniridia, Genitourinary Anomalies and Impaired Intellectual Development Syndrome

Wilms Tumor, Aniridia, Genitourinary Anomalies and Mental Retardation Syndrome

Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation Syndrome

Wilms Tumor-Aniridia-Genitourinary Anomalies-Mental Retardation Syndrome

Wilms Tumor-Aniridia-Genital Anomalies-Retardation Syndrome

Wilms Tumor-Aniridia-Genitourinary Anomalies-Mr Syndrome

Chromosome 11p Deletion Syndrome

Wagr Contiguous Gene Syndrome

Wagr Spectrum Disorder

11p Deletion Syndrome

Wagr Complex

Wagr

Favorite

Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Wilms Tumor, Aniridia, Genitourinary Anomalies, and Impaired Intellectual Development Syndrome, also known as wagr syndrome, is related to wagro syndrome and chromosome 11p deletion, and has symptoms including genitourinary signs and symptoms An important gene associated with Wilms Tumor, Aniridia, Genitourinary Anomalies, and Impaired Intellectual Development Syndrome is WT1 (WT1 Transcription Factor), and among its related pathways/superpathways are Primary ovarian insufficiency and Mesodermal commitment pathway. Affiliated tissues include Kidney and eye, and related phenotypes are aplasia/hypoplasia of the iris and intellectual disability

Related ID：

MALACARDS：WLM020

OMIM：194072

MESH：D017624