| C0000737 |
BXGD000005 |
Abdominal Pain |
Pathological Conditions, Signs and Symptoms |
| C0000768 |
BXGD000007 |
Congenital Abnormality |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C0003962 |
BXGD000244 |
Ascites |
Pathological Conditions, Signs and Symptoms |
| C0004096 |
BXGD000252 |
Asthma |
Respiratory Tract Diseases; Immune System Diseases |
| C0004352 |
BXGD000269 |
Autistic Disorder |
Mental Disorders |
| C0004364 |
BXGD000270 |
Autoimmune Diseases |
Immune System Diseases |
| C0004368 |
BXGD000271 |
Autoimmune state |
|
| C0006142 |
BXGD000374 |
Malignant neoplasm of breast |
Neoplasms; Skin and Connective Tissue Diseases |
| C0006826 |
BXGD000408 |
Malignant Neoplasms |
Neoplasms |
| C0007102 |
BXGD000425 |
Malignant tumor of colon |
Digestive System Diseases; Neoplasms |
| C0007131 |
BXGD000441 |
Non-Small Cell Lung Carcinoma |
Neoplasms; Respiratory Tract Diseases |
| C0007222 |
BXGD000454 |
Cardiovascular Diseases |
Cardiovascular Diseases |
| C0007570 |
BXGD000467 |
Celiac Disease |
Digestive System Diseases; Nutritional and Metabolic Diseases |
| C0008313 |
BXGD000528 |
Cholangitis, Sclerosing |
Digestive System Diseases |
| C0008350 |
BXGD000531 |
Cholelithiasis |
Digestive System Diseases |
| C0008626 |
BXGD000559 |
Congenital chromosomal disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C0009319 |
BXGD000596 |
Colitis |
Digestive System Diseases |
| C0009324 |
BXGD000597 |
Ulcerative Colitis |
Digestive System Diseases |
| C0009447 |
BXGD000613 |
Common Variable Immunodeficiency |
Immune System Diseases |
| C0010346 |
BXGD000664 |
Crohn Disease |
Digestive System Diseases |
| C0011581 |
BXGD000733 |
Depressive disorder |
Mental Disorders |
| C0011847 |
BXGD000749 |
Diabetes |
Endocrine System Diseases |
| C0011849 |
BXGD000751 |
Diabetes Mellitus |
Nutritional and Metabolic Diseases; Endocrine System Diseases |
| C0011854 |
BXGD000753 |
Diabetes Mellitus, Insulin-Dependent |
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases |
| C0011860 |
BXGD000755 |
Diabetes Mellitus, Non-Insulin-Dependent |
Nutritional and Metabolic Diseases; Endocrine System Diseases |
| C0015672 |
BXGD001011 |
Fatigue |
Pathological Conditions, Signs and Symptoms |
| C0015695 |
BXGD001013 |
Fatty Liver |
Digestive System Diseases |
| C0015967 |
BXGD001030 |
Fever |
Pathological Conditions, Signs and Symptoms |
| C0016781 |
BXGD001079 |
Fuchs Endothelial Dystrophy |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C0016978 |
BXGD001087 |
gallbladder neoplasm |
Digestive System Diseases; Neoplasms |
| C0018801 |
BXGD001226 |
Heart failure |
Cardiovascular Diseases |
| C0018802 |
BXGD001227 |
Congestive heart failure |
Cardiovascular Diseases |
| C0019158 |
BXGD001293 |
Hepatitis |
Digestive System Diseases |
| C0019209 |
BXGD001305 |
Hepatomegaly |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C0019214 |
BXGD001307 |
Hepatosplenomegaly |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Hemic and Lymphatic Diseases |
| C0020538 |
BXGD001422 |
Hypertensive disease |
Cardiovascular Diseases |
| C0020541 |
BXGD001424 |
Portal Hypertension |
Digestive System Diseases |
| C0021390 |
BXGD001503 |
Inflammatory Bowel Diseases |
Digestive System Diseases |
| C0022346 |
BXGD001537 |
Icterus |
Pathological Conditions, Signs and Symptoms |
| C0024141 |
BXGD001740 |
Lupus Erythematosus, Systemic |
Skin and Connective Tissue Diseases; Immune System Diseases |
| C0024623 |
BXGD001791 |
Malignant neoplasm of stomach |
Digestive System Diseases; Neoplasms |
| C0025517 |
BXGD001875 |
Metabolic Diseases |
Nutritional and Metabolic Diseases |
| C0027765 |
BXGD002033 |
nervous system disorder |
Nervous System Diseases |
| C0027796 |
BXGD002037 |
Neuralgia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0028754 |
BXGD002082 |
Obesity |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases |
| C0029453 |
BXGD002154 |
Osteopenia |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C0029456 |
BXGD002157 |
Osteoporosis |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C0030193 |
BXGD002191 |
Pain |
Pathological Conditions, Signs and Symptoms |
| C0030305 |
BXGD002206 |
Pancreatitis |
Digestive System Diseases |
| C0032227 |
BXGD002336 |
Pleural effusion disorder |
Respiratory Tract Diseases |
| C0033774 |
BXGD002419 |
Pruritus |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases |
| C0033860 |
BXGD002438 |
Psoriasis |
Skin and Connective Tissue Diseases |
| C0038002 |
BXGD002723 |
Splenomegaly |
Pathological Conditions, Signs and Symptoms |
| C0038013 |
BXGD002725 |
Ankylosing spondylitis |
Musculoskeletal Diseases |
| C0040147 |
BXGD002847 |
Thyroiditis |
Endocrine System Diseases |
| C0042164 |
BXGD002965 |
Uveitis |
Eye Diseases |
| C0042769 |
BXGD002999 |
Virus Diseases |
Infections |
| C0085584 |
BXGD003195 |
Encephalopathies |
Nervous System Diseases |
| C0151872 |
BXGD003493 |
Prothrombin time increased |
Hemic and Lymphatic Diseases |
| C0162557 |
BXGD003956 |
Liver Failure, Acute |
Digestive System Diseases |
| C0200637 |
BXGD004042 |
Monocyte count procedure |
|
| C0200638 |
BXGD004043 |
Eosinophil count procedure |
|
| C0206698 |
BXGD004248 |
Cholangiocarcinoma |
Neoplasms |
| C0239946 |
BXGD005010 |
Fibrosis, Liver |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C0239981 |
BXGD005011 |
Hypoalbuminemia |
Hemic and Lymphatic Diseases |
| C0264009 |
BXGD005361 |
Osteodystrophy |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C0271650 |
BXGD006227 |
Impaired glucose tolerance |
Nutritional and Metabolic Diseases |
| C0278704 |
BXGD006567 |
Malignant Childhood Neoplasm |
Neoplasms |
| C0566602 |
BXGD009489 |
Primary sclerosing cholangitis |
Digestive System Diseases |
| C0596263 |
BXGD009639 |
Carcinogenesis |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0678222 |
BXGD009749 |
Breast Carcinoma |
Neoplasms; Skin and Connective Tissue Diseases |
| C0699790 |
BXGD009866 |
Colon Carcinoma |
Digestive System Diseases; Neoplasms |
| C0699791 |
BXGD009867 |
Stomach Carcinoma |
Digestive System Diseases; Neoplasms |
| C0750880 |
BXGD010239 |
Monocyte count result |
|
| C0871388 |
BXGD011314 |
social stress |
Behavior and Behavior Mechanisms |
| C0920350 |
BXGD011466 |
Autoimmune thyroiditis |
Immune System Diseases; Endocrine System Diseases |
| C1262477 |
BXGD011882 |
Weight decreased |
Pathological Conditions, Signs and Symptoms |
| C1306459 |
BXGD012361 |
Primary malignant neoplasm |
Neoplasms |
| C1319315 |
BXGD012415 |
Adenocarcinoma of large intestine |
Digestive System Diseases; Neoplasms |
| C1389113 |
BXGD012965 |
Generalized amyotrophy |
|
| C1565489 |
BXGD013401 |
Renal Insufficiency |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C1623038 |
BXGD013475 |
Cirrhosis |
Pathological Conditions, Signs and Symptoms |
| C1848701 |
BXGD014967 |
Elevated hepatic transaminase |
|
| C1850959 |
BXGD015188 |
Corneal dystrophy, Fuchs' endothelial, 1 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C2239176 |
BXGD016965 |
Liver carcinoma |
Digestive System Diseases; Neoplasms |
| C2711227 |
BXGD017478 |
Steatohepatitis |
Digestive System Diseases |
| C2931404 |
BXGD018018 |
Albright's hereditary osteodystrophy |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C2931817 |
BXGD018066 |
Chromosome 2q37 deletion syndrome |
Pathological Conditions, Signs and Symptoms |
| C2936476 |
BXGD018123 |
Chronic Liver Failure |
Digestive System Diseases |
| C3150797 |
BXGD018337 |
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 |
|
| C3178766 |
BXGD018535 |
Nociceptive Pain |
Pathological Conditions, Signs and Symptoms |
| C3494506 |
BXGD018968 |
Pseudohypoparathyroidism, Type Ia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C3495559 |
BXGD018994 |
Juvenile arthritis |
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases |
| C4014795 |
BXGD020166 |
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 |
|
| C4020948 |
BXGD020502 |
Palmar telangiectasia |
|
| C4021050 |
BXGD020535 |
Dilated superficial abdominal veins |
|
| C4022766 |
BXGD020993 |
Abnormal large intestine physiology |
|
| C4022867 |
BXGD021019 |
Spider hemangioma |
|
| C4023764 |
BXGD021260 |
Elevated alkaline phosphatase of hepatic origin |
|
| C4025612 |
BXGD021693 |
Polyclonal elevation of IgM |
|
| C4225671 |
BXGD022289 |
VATER/VACTERL ASSOCIATION |
|
| C4310768 |
BXGD022658 |
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 |
|