| C0003507 |
BXGD000203 |
Aortic Valve Stenosis |
Cardiovascular Diseases |
| C0004364 |
BXGD000270 |
Autoimmune Diseases |
Immune System Diseases |
| C0017919 |
BXGD001150 |
Glycogen Storage Disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0020538 |
BXGD001422 |
Hypertensive disease |
Cardiovascular Diseases |
| C0023895 |
BXGD001717 |
Liver diseases |
Digestive System Diseases |
| C0025517 |
BXGD001875 |
Metabolic Diseases |
Nutritional and Metabolic Diseases |
| C0031099 |
BXGD002282 |
Periodontitis |
Stomatognathic Diseases |
| C0086565 |
BXGD003295 |
Liver Dysfunction |
Digestive System Diseases |
| C0152417 |
BXGD003584 |
Congenital stenosis of aortic valve |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C0155567 |
BXGD003803 |
Rheumatic aortic stenosis |
Infections; Cardiovascular Diseases |
| C0231528 |
BXGD004496 |
Myalgia |
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases |
| C0234233 |
BXGD004636 |
Sore to touch |
Pathological Conditions, Signs and Symptoms; Mental Disorders |
| C0241005 |
BXGD005072 |
Creatine phosphokinase serum increased |
|
| C0242379 |
BXGD005157 |
Malignant neoplasm of lung |
Neoplasms; Respiratory Tract Diseases |
| C0270984 |
BXGD006149 |
Metabolic myopathy |
Musculoskeletal Diseases; Nervous System Diseases |
| C0400966 |
BXGD008266 |
Non-alcoholic Fatty Liver Disease |
Digestive System Diseases |
| C0424551 |
BXGD008533 |
Impaired exercise tolerance |
|
| C0427460 |
BXGD008616 |
Red cell distribution width determination |
|
| C0684249 |
BXGD009790 |
Carcinoma of lung |
Neoplasms; Respiratory Tract Diseases |
| C1265996 |
BXGD011927 |
Large cell neuroendocrine carcinoma |
Neoplasms |
| C1304746 |
BXGD012343 |
RDW - Red blood cell distribution width result |
|
| C1306460 |
BXGD012362 |
Primary malignant neoplasm of lung |
Neoplasms; Respiratory Tract Diseases |
| C1968729 |
BXGD016730 |
Increased muscle glycogen content |
|
| C2752027 |
BXGD017755 |
Glycogen Storage Disease XIII |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |