Informaţii despre

Nume Wilms Tumor 6
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli rare; Bolile canceroase
Clasificare anatomică Malacards Boli nefrologice (ale rinichilor)
Boli din aceeaşi familie Familial Wilms Tumor 2; Wilms Tumor 1; Wilms Tumor 2; Wilms Tumor 3; Wilms Tumor 4; Wilms Tumor 5

Vezi şi

Boli A-Z 46 Xy Gonadal Dysgenesis 46,xy Sex Reversal 3 9q22.3 Microdeletion Acquired Von Willebrand Syndrome Acromelic Frontonasal Dysostosis Acute Leukemia Acute Lymphoblastic Leukemia, Childhood Acute Lymphocytic Leukemia Acute Promyelocytic Leukemia Adenocarcinoma Adenofibroma Adenoma Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete Adrenal Neuroblastoma Aging Alagille Syndrome 1 Alpha-Fetoprotein Deficiency Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Anauxetic Dysplasia 1 Aniridia 1 Anorexia Nervosa 1 Appendicitis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Astrocytoma Ataxia and Polyneuropathy, Adult-Onset Ataxia-Telangiectasia Autoimmune Lymphoproliferative Syndrome, Type V Azoospermia Beckwith-Wiedemann Syndrome Bilateral Retinoblastoma Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Bloom Syndrome Bohring-Opitz Syndrome Botryoid Rhabdomyosarcoma Breast Cancer Cataract Cerebellar Angioblastoma Cerebritis Cervical Polyp Cervicitis Childhood Leukemia Chromosomal Triplication Chromosome 11p Deletion Chronic Leukemia Ciliary Dyskinesia, Primary, 1 Clear Cell Adenocarcinoma Clear Cell Sarcoma Cloacogenic Carcinoma Colorblindness, Partial, Protan Series Colorectal Adenocarcinoma Colorectal Cancer Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Anomalies of Kidney and Urinary Tract 2 Congenital Mesoblastic Nephroma Cornelia De Lange Syndrome Cranioectodermal Dysplasia 1 Cryptococcosis Cystic Nephroma Cytogenetically Normal Acute Myeloid Leukemia Denys-Drash Syndrome Dermatofibrosarcoma Protuberans Dermoid Cyst Desmoid Tumor Desmoplastic Small Round Cell Tumor Diabetes Insipidus Diaphanospondylodysostosis Diarrhea 5, with Tufting Enteropathy, Congenital Diastematomyelia Diffuse Mesangial Sclerosis Down Syndrome Embryonal Carcinoma Embryonal Rhabdomyosarcoma Encephalocraniocutaneous Lipomatosis Encephalopathy Endometrial Adenocarcinoma Endometriosis Endotheliitis End Stage Renal Failure Epignathus Epithelial Recurrent Erosion Dystrophy Esophageal Cancer Estrogen Resistance Extragonadal Teratoma Factor Vii Deficiency Familial Wilms Tumor 2 Fibromatosis Fibrosarcoma Focal Segmental Glomerulosclerosis Frasier Syndrome Ganglioneuroblastoma Ganglioneuroma Gastric Cancer Gastroenteritis Germ Cells Tumors Gigantism Glioblastoma Glioma Glomerulonephritis Gonadal Dysgenesis Gonadoblastoma Headache Helix Syndrome Hematopoietic Stem Cell Transplantation Hemihyperplasia, Isolated Hemophagocytic Lymphohistiocytosis Hepatic Adenomas, Familial Hepatic Encephalopathy Hepatic Veno-Occlusive Disease Hepatitis Hepatoblastoma Hepatocellular Carcinoma Hereditary Spherocytosis Hereditary Wilms' Tumor Hermaphroditism Histiocytosis Horseshoe Kidney Hydrocele Hydronephrosis Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant Hypereosinophilic Syndrome Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Encephalopathy Hypospadias Hypoxia Incontinentia Pigmenti Inflammatory Myofibroblastic Tumor Insulin-Like Growth Factor I Intestinal Perforation Klippel-Trenaunay-Weber Syndrome L-2-Hydroxyglutaric Aciduria Lambert-Eaton Myasthenic Syndrome Langerhans Cell Histiocytosis Langerhans Cell Sarcoma Leiomyoma Leukemia Lipomatosis Lung Cancer Lung Disease Lymphangioma Lymphoblastic Leukemia Lymphoma Malignant Glioma Malignant Peripheral Nerve Sheath Tumor Malignant Pleural Mesothelioma Measles Medulloblastoma Melanoma Membranoproliferative Glomerulonephritis Mental Retardation-Hypotonic Facies Syndrome, X-Linked, 1 Metanephric Adenoma Microcephaly Miller-Dieker Lissencephaly Syndrome Mulibrey Nanism Multilocular Cystic Renal Neoplasm of Low Malignant Potential Multiloculated Renal Cyst Mumps Mycobacterium Fortuitum Myelodysplastic Syndrome Myelofibrosis Myeloid Leukemia Myeloproliferative Neoplasm Nephrotic Syndrome Nephrotic Syndrome, Type 4 Neuroblastoma Neurofibromatosis, Type Iv, of Riccardi Neurofibrosarcoma Neuronitis Nicolaides-Baraitser Syndrome Nodular Regenerative Hyperplasia Oncocytoma Oral Cancer Oral Squamous Cell Carcinoma Orofacial Cleft Osteonecrosis Osteopathia Striata with Cranial Sclerosis Osteopetrosis Ovarian Cancer Ovarian Cyst Pancreatic Cancer Pancreatic Ductal Adenocarcinoma Pancreatitis Papillary Adenocarcinoma Paraneoplastic Syndromes Peritonitis Perlman Syndrome Persistent Idiopathic Facial Pain Phace Syndrome Phacomatosis Pigmentokeratotica Pheochromocytoma Pik3ca-Related Overgrowth Spectrum Pneumonia Polycystic Ovary Syndrome Polycythemia Polydactyly Polykaryocytosis Inducer Polymicrogyria, Bilateral Perisylvian, X-Linked Portal Hypertension Premature Centromere Division Prostate Cancer Prostatitis Pseudohermaphroditism Pulmonary Embolism Pulmonary Fibrosis Pyelonephritis Renal Dysplasia Renal Tubular Acidosis Retinoblastoma Rhabdomyosarcoma Rhabdomyosarcoma, Embryonal, 1 Ring Chromosome 11 Roberts Syndrome Rubella Sacrococcygeal Teratoma Sarcoma Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Skin Epithelioid Hemangioma Skull Base Meningioma Smith-Kingsmore Syndrome Soft Tissue Sarcoma Spondylocarpotarsal Synostosis Syndrome Spondyloocular Syndrome Squamous Cell Carcinoma Teratoma Testicular Germ Cell Tumor Testicular Germ Cell Tumor 1 Thrombocytopenia Thrombosis Thymic Hyperplasia Thyroid Cancer Thyroiditis Toxocariasis Tuberous Sclerosis Tumor Suppressor Gene on Chromosome 11 Urticaria Urticaria Pigmentosa Uterine Anomalies Uterine Carcinosarcoma Uterine Sarcoma Vacterl Association, X-Linked, with or Without Hydrocephalus Vasculitis Wells Syndrome Whim Syndrome Williams-Beuren Syndrome Wilms Tumor 1 Wilms Tumor 2 Wilms Tumor 3 Wilms Tumor 4 Wilms Tumor 5 Wilms Tumor, Aniridia, Genitourinary Anomalies, and Mental Retardation Syndrome Wilms Tumor Predisposition Wilson-Turner X-Linked Mental Retardation Syndrome Xanthogranulomatous Pyelonephritis