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
Laryngomalacia. Laryngomalacias . Larynx Chondromalacia . Larynx Chondromalacias . Chondromalacia of Larynx . A congenital or acquired condition of underdeveloped or degeneration of CARTILAGE in the LARYNX. This results in a floppy laryngeal wall making patency difficult to maintain. . 0.79
Tracheomalacia. Trachea Chondromalacia . Trachea Chondromalacias . Tracheomalacias . Chondromalacia of Trachea . A congenital or acquired condition of underdeveloped or degeneration of CARTILAGE in the TRACHEA. This results in a floppy tracheal wall making patency difficult to maintain. It is characterized by wheezing and difficult breathing. . 0.61
Bronchomalacia. Bronchi Chondromalacia . Bronchi Chondromalacias . Bronchomalacias . Chondromalacia of Bronchi . A congenital or acquired condition of underdeveloped or degeneration of CARTILAGE in the BRONCHI. This results in a floppy bronchial wall making patency difficult to maintain. It is characterized by wheezing and difficult breathing. . 0.59
Patient Education Handout. Consumer Handout . Consumer Information Handout . Consumer Information Handout . Consumer Information Handout [Publication Type] . Patient Education Handout [Publication Type] . Works consisting of a handout or self-contained informative material used to explain a procedure or a condition or the contents of a specific article in a biomedical journal and written in non-technical language for the patient or consumer. . 0.42
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Gain of Function Mutation. Activation Mutation . Activation Mutations . Mutation, Activation . Mutations, Activation . A mutation that results in an increase in a gene's activity or in acquiring a new molecular function or a new pattern of gene expression. . 0.34
Airway Management. Airway Control . Control, Airway . Management, Airway . Evaluation, planning, and use of a range of procedures and airway devices for the maintenance or restoration of a patient's ventilation. . 0.34
Splints. Dynamic Orthoses . Dynamic Splint . Dynamic Splinting . Dynamic Splints . Static Orthoses . Static Splint . Static Splinting . Static Splints . Dynamic Splintings . Splint . Splint, Dynamic . Splint, Static . Splinting, Dynamic . Splinting, Static . Splints, Dynamic . Splints, Static . Static Orthose . Rigid or flexible appliances that are used to maintain a displaced or movable part in position, or to maintain the position of and protect an injured part. . 0.33
Trismus. Lock Jaw . Masseter Spasm . Masseter Muscle Spasms . Masseter Spasms . Muscle Spasm, Masseter . Muscle Spasms, Masseter . Spasm, Masseter . Spasm, Masseter Muscle . Spasms, Masseter . Spasms, Masseter Muscle . Lockjaw . Masseter Muscle Spasm . Spasmodic contraction of the masseter muscle resulting in forceful jaw closure. This may be seen with a variety of diseases, including TETANUS, as a complication of radiation therapy, trauma, or in association with neoplastic conditions. . 0.33
Gynatresia. Asherman's Syndrome . Intrauterine Synechiae . Uterine Synechiae . Ashermans Syndrome . Gynatresias . Syndrome, Asherman . Syndrome, Asherman's . Synechiae, Intrauterine . Synechiae, Uterine . Asherman Syndrome . Absence of a normal opening in the lumen of the female genital tract, from the FALLOPIAN TUBES to the VAGINA. This anomaly may be congenital or acquired due to injuries, diseases, or TISSUE ADHESIONS. . 0.33
