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wagr syndromes
(phenotype)
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WAGRO
PRAME
HBAP1
CLIC5
APOA1
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Pathway Enrichment
Most Correlated Biogroups
LI_WILMS_TUMOR_VS_FETAL_KIDNEY_1_UP
FLECHNER_BIOPSY_KIDNEY_TRANSPLANT_REJECTED_VS_OK_DN
MODULE_55
extracellular vesicle
MODULE_88
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There were no matches for wagr syndromes
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Characterization of WAGR Syndrome and Other Chromosome 11 Gene Deletions
Genetic Overlap Between Anomalies and Cancer in Kids in the Children's Oncology Group: The COG GOBAC…
Registry for Patients With Wilms' Tumor Suppressor Gene 1 (WT1) Mutation Associated Diseases
Congenital Aniridia Patient Questionnaire
Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford
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