serw-MX  [xml]
Williams Campbell Syndrome CID10 - Classificação Internacional de Doenças DeCS Português DeCS Inglês DeCS Espanhol DeCS Espanha DeCS Português com escopo DeCS Inglês com escopo DeCS Espanhol com escopo DeCS Espanha com escopo LILACS - LILACS Regional
DeCS Categories C05 Musculoskeletal Diseases . C05.182 Cartilage Diseases . C05.182.895 Tracheobronchomalacia . C08 Respiratory Tract Diseases . C08.127 Bronchial Diseases . C08.127.719 Tracheobronchomalacia . C08.907 Tracheal Diseases . C08.907.796 Tracheobronchomalacia . C10 Nervous System Diseases . C10.597 Neurologic Manifestations . C10.597.606 Neurobehavioral Manifestations . C10.597.606.643 Intellectual Disability . C10.597.606.643.970 Williams Syndrome . C14 Cardiovascular Diseases . C14.280 Heart Diseases . C14.280.484 Heart Valve Diseases . C14.280.484.150 Aortic Valve Stenosis . C14.280.484.150.535 Aortic Stenosis, Supravalvular . C14.280.484.150.535.960 Williams Syndrome . C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities . C16.131 Congenital Abnormalities . C16.131.260 Chromosome Disorders . C16.131.260.970 Williams Syndrome . C16.131.621 Musculoskeletal Abnormalities . C16.131.621.953 Tracheobronchomalacia . C16.320 Genetic Diseases, Inborn . C16.320.180 Chromosome Disorders . C16.320.180.970 Williams Syndrome . C17 Skin and Connective Tissue Diseases . C17.300 Connective Tissue Diseases . C17.300.182 Cartilage Diseases . C17.300.182.895 Tracheobronchomalacia .		Terms  Synonyms & Historicals Documents LILACS e MDL   Tracheobronchomalacia . Williams-Campbell Syndrome . Syndrome, Williams-Campbell . Tracheobronchomalacias . Williams Campbell Syndrome . Chondromalacia of Trachea and Bronchi . A congenital or acquired condition of underdeveloped or degeneration of CARTILAGE in the TRACHEA and the BRONCHI. This results in a floppy non-rigid airway making patency difficult to maintain. . 1.00 3 129   Williams Syndrome . Beuren Syndrome . Chromosome 7q11.23 Deletion Syndrome . Hypercalcemia-Supravalvar Aortic Stenosis . Supravalvar Aortic Stenosis Syndrome . Williams Contiguous Gene Syndrome . Williams-Beuren Syndrome . Aortic Stenoses, Hypercalcemia-Supravalvar . Aortic Stenosis, Hypercalcemia-Supravalvar . Hypercalcemia Supravalvar Aortic Stenosis . Hypercalcemia-Supravalvar Aortic Stenoses . Stenoses, Hypercalcemia-Supravalvar Aortic . Stenosis, Hypercalcemia-Supravalvar Aortic . Syndrome, Beuren . Syndrome, Williams . Syndrome, Williams-Beuren . Williams Beuren Syndrome . Contiguous Gene Syndrome, Williams . Elfin Facies Syndrome . WILLIAMS-BEUREN SYNDROME . A disorder caused by hemizygous microdeletion of about 28 genes on chromosome 7q11.23, including the ELASTIN gene. Clinical manifestations include SUPRAVALVULAR AORTIC STENOSIS; MENTAL RETARDATION; elfin facies; impaired visuospatial constructive abilities; and transient HYPERCALCEMIA in infancy. The condition affects both sexes, with onset at birth or in early infancy. . 0.72