Informaţii despre

Nume Beckwith-Wiedemann Syndrome
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli rare
Clasificari ICD10 Congenital malformation syndromes involving early overgrowth
Clasificare anatomică Malacards Boli nefrologice (ale rinichilor)
Boli din aceeaşi familie Beckwith-Wiedemann Syndrome Due to 11p15 Translocation/inversion; Beckwith-Wiedemann Syndrome Due to Imprinting Defect of 11p15; Beckwith-Wiedemann Syndrome Due to Paternal Uniparental Disomy of Chromosome 11

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Boli A-Z Abdominal Wall Defect Acid-Labile Subunit Deficiency Acid Sphingomyelinase Deficiency Acute Lymphocytic Leukemia Adenoma Adrenal Adenoma Adrenal Cortical Adenoma Adrenal Neuroblastoma Adrenocortical Carcinoma, Hereditary Adult Syndrome Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha-Fetoprotein Deficiency Alport Syndrome, X-Linked Al-Raqad Syndrome Androgen Insensitivity Syndrome, Mild Aniridia 1 Ankyloglossia Anorexia Nervosa 1 Arteriovenous Malformation Arthrochalasia Ehlers-Danlos Syndrome Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia Neuropathy Spectrum Atypical Teratoid Rhabdoid Tumor Beckwith-Wiedemann Syndrome Due to Imprinting Defect of 11p15 Biliary Hypoplasia Birt-Hogg-Dube Syndrome Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 Breast Fibroadenoma Cerebellar Angioblastoma Chorioangioma Choroiditis Chromosomal Triplication Chromosome 11p Duplication Congenital Hypothyroidism Congenital Mesoblastic Nephroma Congenital Pancreatic Cyst Costello Syndrome Cystic Fibrosis Cystinuria Diabetes Mellitus Diabetes Mellitus, Transient Neonatal, 1 Diaphragmatic Eventration Diencephalic Syndrome Encephalocele Esophageal Atresia Factor Vii Deficiency Fanconi-Bickel Syndrome Fetal Macrosomia Gestational Trophoblastic Neoplasm Gigantism Glioma Hemangioendothelioma Hemangioma Hemihyperplasia, Isolated Hepatitis Hepatoblastoma Hereditary Wilms' Tumor Hydatidiform Mole, Recurrent, 1 Hyperinsulinemic Hypoglycemia Hyperinsulinemic Hypoglycemia, Familial, 2 Hyperinsulinemic Hypoglycemia, Familial, 3 Hyperinsulinemic Hypoglycemia, Familial, 4 Hyperinsulinism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrophic Cardiomyopathy Hypoglycemia Hypopituitarism Incontinentia Pigmenti Intraneural Perineurioma Intussusception Jacobsen Syndrome Kagami-Ogata Syndrome Kidney Cancer Kidney Sarcoma Laryngitis Leukemia Long Qt Syndrome Lymphedema Macroglossia Medullary Sponge Kidney Megakaryocytic Leukemia Melanoma Mismatch Repair Cancer Syndrome Mosaic Genome-Wide Paternal Uniparental Disomy Muscular Dystrophy, Duchenne Type Myeloid Leukemia Myoclonus Nasal Encephalocele Neonatal Diabetes Mellitus Neural Crest Tumor Neuroblastoma Nipples, Supernumerary Omphalocele Orbit Rhabdomyosarcoma Palmoplantar Keratoderma, Epidermolytic Pancreatitis Pancreatoblastoma Perineurioma Perlman Syndrome Persistent Idiopathic Facial Pain Pheochromocytoma Pituitary Adenoma Posterior Urethral Valves Preeclampsia/eclampsia 4 Preeclampsia/eclampsia 5 Prune Belly Syndrome Pseudohypoparathyroidism Pseudohypoparathyroidism, Type Ib Pyoderma Pyoderma Gangrenosum Renal Dysplasia Rhabdoid Cancer Rhabdomyosarcoma Schizencephaly Scoliosis Sensorineural Hearing Loss 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 Sleep Disorder Sotos Syndrome 1 Spastic Paraplegia 17, Autosomal Dominant Spindle Cell Liposarcoma Subvalvular Aortic Stenosis Teratoma Testicular Malignant Germ Cell Cancer Tetralogy of Fallot Thymic Hyperplasia Type 1 Diabetes Mellitus 2 Umbilical Hernia Urethritis Urinary System Disease Ventricular Fibrillation, Paroxysmal Familial, 1 Whim Syndrome Williams-Beuren Syndrome Wilms Tumor 1 Wilms Tumor 5 Wilms Tumor 6 Wilson-Turner X-Linked Mental Retardation Syndrome