Informaţii despre

Nume Wilms Tumor 5
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 6

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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 Alpha-Fetoprotein Deficiency Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Anauxetic Dysplasia 1 Aniridia 1 Anorexia Nervosa 1 Anterior Segment Dysgenesis 1 Appendicitis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Arthropathy, Progressive Pseudorheumatoid, of Childhood Astrocytoma Ataxia and Polyneuropathy, Adult-Onset Ataxia-Telangiectasia Autoimmune Lymphoproliferative Syndrome, Type V Azoospermia Beckwith-Wiedemann Syndrome Beckwith-Wiedemann Syndrome Due to Imprinting Defect of 11p15 Bilateral Retinoblastoma Bladder Benign Neoplasm 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 Endodermal Sinus Tumor Childhood Leukemia Chromosomal Triplication Chromosome 11p Deletion Chronic Leukemia Ciliary Dyskinesia, Primary, 1 Clear Cell Adenocarcinoma Clear Cell Sarcoma Colorblindness, Partial, Protan Series Colorectal Adenocarcinoma Colorectal Cancer Congenital Anomalies of Kidney and Urinary Tract 2 Congenital Aphakia Congenital Mesoblastic Nephroma Cornelia De Lange Syndrome Cranioectodermal Dysplasia 1 Cryptococcosis Cystic Nephroma Cytogenetically Normal Acute Myeloid Leukemia Deafness, Autosomal Dominant 10 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 Endocervical Adenocarcinoma Endometrial Adenocarcinoma Endometriosis Endosalpingiosis Endotheliitis End Stage Renal Failure Epithelial Recurrent Erosion Dystrophy Esophageal Cancer Estrogen Resistance Factor Vii Deficiency Familial Wilms Tumor 2 Female Reproductive Endometrioid Cancer Fibrosarcoma Focal Segmental Glomerulosclerosis Frasier Syndrome Frozen Shoulder 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 Hepatitis Hepatoblastoma Hepatocellular Carcinoma Hereditary Spherocytosis Hereditary Wilms' Tumor Horseshoe Kidney Hydatidiform Mole, Recurrent, 1 Hydrocele 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 Iris Disease Kidney Cancer Klippel-Trenaunay-Weber Syndrome L-2-Hydroxyglutaric Aciduria Lambert-Eaton Myasthenic Syndrome 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 Mumps Mycobacterium Fortuitum Myelodysplastic Syndrome Myelofibrosis Myeloid Leukemia Myeloproliferative Neoplasm Nephrogenic Adenofibroma Nephrogenic Adenoma Nephrogenic Adenoma of Urinary Bladder Nephrotic Syndrome Nephrotic Syndrome, Type 4 Neuroblastoma Neurofibromatosis, Type Iv, of Riccardi Neurofibrosarcoma Neuronitis Nodular Regenerative Hyperplasia Oral Cancer Oral Squamous Cell Carcinoma Orofacial Cleft Osteopathia Striata with Cranial Sclerosis Ovarian Brenner Tumor Ovarian Cancer Ovarian Cyst Pancreatic Cancer Pancreatic Ductal Adenocarcinoma Pancreatitis Papillary Adenocarcinoma Papillorenal Syndrome Paraneoplastic Syndromes Pauci-Immune Glomerulonephritis Peritoneum Cancer Peritonitis Perlman Syndrome Persistent Idiopathic Facial Pain Phace Syndrome Pheochromocytoma Pik3ca-Related Overgrowth Spectrum Pneumonia Polycystic Ovary Syndrome Polydactyly Polykaryocytosis Inducer Polymicrogyria, Bilateral Perisylvian, X-Linked Portal Hypertension Premature Centromere Division Prostate Cancer Prostatitis Pseudohermaphroditism Pseudopapilledema Pulmonary Fibrosis Pyelonephritis Renal Adenoma Renal Dysplasia Renal Tubular Acidosis Rete Testis Adenoma Retinoblastoma Rhabdomyosarcoma Rhabdomyosarcoma, Embryonal, 1 Ring Chromosome 11 Roberts Syndrome Rubella Sacrococcygeal Teratoma Sarcoma Scleral Staphyloma Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Silver-Russell Syndrome Silver-Russell Syndrome Due to 11p15 Microduplication Silver-Russell Syndrome Due to an Imprinting Defect of 11p15 Silver-Russell Syndrome Due to a Point Mutation Simpson-Golabi-Behmel Syndrome Skin Epithelioid Hemangioma Skull Base Meningioma Smith-Kingsmore Syndrome Soft Tissue Sarcoma Spastic Paraplegia 17, Autosomal Dominant Spondylocarpotarsal Synostosis Syndrome Spondyloocular Syndrome Squamous Cell Carcinoma Teratoma Testicular Germ Cell Tumor Testicular Germ Cell Tumor 1 Thrombocytopenia Thymic Hyperplasia Thyroid Cancer Thyroiditis Toxocariasis Tuberous Sclerosis Tumor Suppressor Gene on Chromosome 11 Umbilical Hernia Urethral Diverticulum Urticaria Urticaria Pigmentosa Uterine Anomalies Uterine Carcinosarcoma Uterine Sarcoma Vasculitis Whim Syndrome Williams-Beuren Syndrome Wilms Tumor 1 Wilms Tumor 2 Wilms Tumor 3 Wilms Tumor 4 Wilms Tumor 6 Wilms Tumor and Radial Bilateral Aplasia Wilms Tumor, Aniridia, Genitourinary Anomalies, and Mental Retardation Syndrome Wilms Tumor Predisposition Wilson-Turner X-Linked Mental Retardation Syndrome Xanthogranulomatous Pyelonephritis