disease has basis in dysfunction of H19 hereditary Wilms tumor Wilms tumor 2 FWT2 GARD:0008559 MESH:C536853 MONDO:0008680 OMIM:194071 WT2 Wilms tumor 2 Wilms tumor type 2 familial Wilms tumor 2 https://rarediseases.info.nih.gov/diseases/8559/familial-wilms-tumor-2