WAGR Syndrome
WAGR Syndrome
About the Disease
Wilms Tumor, Aniridia, Genitourinary Anomalies, and Mental Retardation Syndrome, also known as wagr syndrome, is related to aniridia 2 and gillespie syndrome, and has symptoms including genitourinary signs and symptoms An important gene associated with Wilms Tumor, Aniridia, Genitourinary Anomalies, and Mental Retardation Syndrome is WT1 (WT1 Transcription Factor), and among its related pathways/superpathways are Mesodermal commitment pathway and BMP signaling in eyelid development. Affiliated tissues include Kidney, eye and testes, and related phenotypes are aplasia/hypoplasia of the iris and aniridia
Common Targets
PAX6 | LDHD

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Chloridorrhea, Congenital | Arthrogryposis | Osteogenesis Imperfecta Type IV | Spinocerebellar Ataxia Type 20 | Spinocerebellar Ataxia Type 15 | Vestibular Disease | Loeys-Dietz Syndrome | Atelosteogenesis Type 1 | Rheumatic Heart Disease | Auriculocondylar Syndrome | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Ectodermal Dysplasia | Congenital Torticollis | Salla Disease | Pierson Syndrome | Cystinosis | Hydrocephalus, Normal Pressure | Pycnodysostosis | Giant Axonal Neuropathy | Sezary Syndrome | Renal Oncocytoma | Conduct Disorder | Brooke-Spiegler Syndrome | Polycystic Kidney, Autosomal Dominant | Fetal And Neonatal Alloimmune Thrombocytopenia | Retinopathy Of Prematurity | Hypercholesterolemia | Obsessive-compulsive Disorder | Episodic Ataxia Type 2 | Coloboma | Aplastic Anemia | Craniometaphyseal Dysplasia | Familial Dysautonomia | Granuloma Annulare | Hydrocephalus | Glutaric Aciduria Type 2 | Irritable Bowel Syndrome | Mountain Sickness | Long-chain 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