serw-MX  [xml]  

 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 .
 Synonyms & Historicals
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. .
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 .
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. .