Informaţii despre

Nume Williams-Beuren Syndrome
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli rare
Clasificari ICD10 Other specified congenital malformation syndromes, not elsewhere classified
Clasificare anatomică Malacards Boli ale ochiului; Boli cardiovasculare; Boli nefrologice (ale rinichilor); Boli neuronale

Vezi şi

Boli A-Z 7q11.23 Duplication Syndrome Achalasia Acquired Von Willebrand Syndrome Adenocarcinoma Aging Alacrima, Achalasia, and Mental Retardation Syndrome Alagille Syndrome 1 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Amusia Anaplastic Oligodendroglioma Aneurysm Aniridia 1 Anorexia Nervosa 1 Aortic Coarctation Aortic Valve Disease 2 Arteries, Anomalies of Arthrochalasia Ehlers-Danlos Syndrome Astrocytoma Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Atrioventricular Septal Defect Attention Deficit-Hyperactivity Disorder Autism Autism Spectrum Disorder Autoimmune Disease Ayme-Gripp Syndrome Beckwith-Wiedemann Syndrome Biliary Hypoplasia 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 Brain Injury Branchiootic Syndrome 1 Burkitt Lymphoma Cardiac Arrest Celiac Disease 1 Central Precocious Puberty Cerebellar Atrophy, Developmental Delay, and Seizures Cerebritis Cervicitis Charge Syndrome Chromosomal Deletion Syndrome Chromosomal Triplication Chromosome 7q11.23 Deletion Syndrome, Distal, 1.2-Mb Chronic Granulomatous Disease Cognitive Function 1, Social Complete Atrioventricular Canal Cone Dystrophy Congenital Hypothyroidism Coronary Artery Anomaly Craniosynostosis Crohn's Colitis Crohn's Disease Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome Discrete Subaortic Stenosis Diverticulitis Down Syndrome Dysphagia Dysphasia, Familial Developmental Ebstein Anomaly Emphysema, Congenital Lobar Encephalopathy Endocarditis Epilepsy Esotropia Essential Iris Atrophy Facial Dysmorphism-Anorexia-Cachexia-Eye and Skin Anomalies Syndrome Fanconi Anemia, Complementation Group E Fetishism Fragile X Syndrome Gianotti Crosti Syndrome Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies Glucose Intolerance Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I Growth Hormone Deficiency Helix Syndrome Hyperacusis Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Encephalopathy Hypertrophic Cardiomyopathy Hypothyroidism, Congenital, Nongoitrous, 2 Idiopathic Infantile Hypercalcemia Inflammatory Bowel Disease 1 Inguinal Hernia Keratoconus Learning Disability Leukemia Lipedema Lipoid Proteinosis of Urbach and Wiethe Long Qt Syndrome Lymphoid Interstitial Pneumonia Lymphoma Malignant Hyperthermia Malignant Spiradenoma Meckel Syndrome, Type 1 Microcephaly Moebius Syndrome Multiple Sclerosis Musical Perfect Pitch Myocardial Infarction Myopathy Neurodegeneration with Brain Iron Accumulation 2a Neurofibromatosis, Type Iv, of Riccardi Neuronitis Nipples, Supernumerary Oculocerebral Syndrome with Hypopigmentation Oculoectodermal Syndrome Oligodendroglioma Otitis Media Periodontitis Periventricular Nodular Heterotopia Phelan-Mcdermid Syndrome Phobia, Specific Phosphoserine Phosphatase Deficiency Pilomyxoid Astrocytoma Portal Hypertension Prader-Willi Syndrome Precocious Puberty Pulmonary Sequestration Pulmonary Valve Stenosis Radioulnar Synostosis Renal Dysplasia Sacral Defect with Anterior Meningocele Schizophrenia Scoliosis Sensorineural Hearing Loss Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Sotos Syndrome 1 Specific Language Impairment Strabismus Succinic Semialdehyde Dehydrogenase Deficiency Supravalvular Aortic Stenosis Synostosis Thyroiditis Tibia, Hypoplasia or Aplasia of, with Polydactyly Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Turner Syndrome Vascular Disease Velocardiofacial Syndrome Waldenstrom Macroglobulinemia Weill-Marchesani Syndrome Werner Syndrome West Syndrome Wilms Tumor 6