| C0002873 |
BXGD000133 |
Anemia of chronic disease |
Hemic and Lymphatic Diseases |
| C0004096 |
BXGD000252 |
Asthma |
Respiratory Tract Diseases; Immune System Diseases |
| C0004352 |
BXGD000269 |
Autistic Disorder |
Mental Disorders |
| C0005890 |
BXGD000345 |
Body Height |
|
| C0006142 |
BXGD000374 |
Malignant neoplasm of breast |
Neoplasms; Skin and Connective Tissue Diseases |
| C0006287 |
BXGD000390 |
Bronchopulmonary Dysplasia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases |
| C0006826 |
BXGD000408 |
Malignant Neoplasms |
Neoplasms |
| C0007102 |
BXGD000425 |
Malignant tumor of colon |
Digestive System Diseases; Neoplasms |
| C0007113 |
BXGD000430 |
Rectal Carcinoma |
Digestive System Diseases; Neoplasms |
| C0007134 |
BXGD000443 |
Renal Cell Carcinoma |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0008479 |
BXGD000544 |
Chondrosarcoma |
Neoplasms |
| C0009402 |
BXGD000605 |
Colorectal Carcinoma |
Digestive System Diseases; Neoplasms |
| C0009782 |
BXGD000631 |
Connective Tissue Diseases |
Skin and Connective Tissue Diseases |
| C0010068 |
BXGD000648 |
Coronary heart disease |
Cardiovascular Diseases |
| C0011303 |
BXGD000712 |
Demyelinating Diseases |
Nervous System Diseases |
| C0011644 |
BXGD000744 |
Scleroderma |
Skin and Connective Tissue Diseases |
| C0011847 |
BXGD000749 |
Diabetes |
Endocrine System Diseases |
| C0011849 |
BXGD000751 |
Diabetes Mellitus |
Nutritional and Metabolic Diseases; Endocrine System Diseases |
| C0011853 |
BXGD000752 |
Diabetes Mellitus, Experimental |
Nutritional and Metabolic Diseases; Endocrine System Diseases |
| C0013404 |
BXGD000833 |
Dyspnea |
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases |
| C0013743 |
BXGD000862 |
Eisenmenger Complex |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C0014060 |
BXGD000882 |
Encephalitis, St. Louis |
Infections; Nervous System Diseases |
| C0016667 |
BXGD001072 |
Fragile X Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0017638 |
BXGD001132 |
Glioma |
Neoplasms |
| C0018213 |
BXGD001187 |
Graves Disease |
Eye Diseases; Immune System Diseases; Endocrine System Diseases |
| C0018799 |
BXGD001224 |
Heart Diseases |
Cardiovascular Diseases |
| C0018801 |
BXGD001226 |
Heart failure |
Cardiovascular Diseases |
| C0018802 |
BXGD001227 |
Congestive heart failure |
Cardiovascular Diseases |
| C0018816 |
BXGD001234 |
Heart Septal Defects |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C0018817 |
BXGD001235 |
Atrial Septal Defects |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C0019079 |
BXGD001278 |
Hemoptysis |
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases |
| C0019196 |
BXGD001301 |
Hepatitis C |
Digestive System Diseases; Infections |
| C0019693 |
BXGD001346 |
HIV Infections |
Infections; Immune System Diseases |
| C0020459 |
BXGD001394 |
Hyperinsulinism |
Nutritional and Metabolic Diseases |
| C0020507 |
BXGD001413 |
Hyperplasia |
Pathological Conditions, Signs and Symptoms |
| C0020538 |
BXGD001422 |
Hypertensive disease |
Cardiovascular Diseases |
| C0020542 |
BXGD001425 |
Pulmonary Hypertension |
Respiratory Tract Diseases |
| C0020676 |
BXGD001462 |
Hypothyroidism |
Endocrine System Diseases |
| C0021704 |
BXGD001510 |
Intelligence |
Behavior and Behavior Mechanisms |
| C0023467 |
BXGD001658 |
Leukemia, Myelocytic, Acute |
Neoplasms |
| C0024117 |
BXGD001734 |
Chronic Obstructive Airway Disease |
Respiratory Tract Diseases |
| C0024141 |
BXGD001740 |
Lupus Erythematosus, Systemic |
Skin and Connective Tissue Diseases; Immune System Diseases |
| C0024790 |
BXGD001804 |
Paroxysmal nocturnal hemoglobinuria |
Hemic and Lymphatic Diseases |
| C0025202 |
BXGD001832 |
melanoma |
Neoplasms |
| C0025322 |
BXGD001863 |
Premature Menopause |
Female Urogenital Diseases and Pregnancy Complications |
| C0025517 |
BXGD001875 |
Metabolic Diseases |
Nutritional and Metabolic Diseases |
| C0026654 |
BXGD001914 |
Moyamoya Disease |
Nervous System Diseases; Cardiovascular Diseases |
| C0026769 |
BXGD001930 |
Multiple Sclerosis |
Immune System Diseases; Nervous System Diseases |
| C0027627 |
BXGD002006 |
Neoplasm Metastasis |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0027651 |
BXGD002009 |
Neoplasms |
Neoplasms |
| C0027819 |
BXGD002043 |
Neuroblastoma |
Neoplasms |
| C0028754 |
BXGD002082 |
Obesity |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases |
| C0029463 |
BXGD002160 |
Osteosarcoma |
Neoplasms |
| C0032460 |
BXGD002355 |
Polycystic Ovary Syndrome |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C0033578 |
BXGD002408 |
Prostatic Neoplasms |
Neoplasms; Male Urogenital Diseases |
| C0034069 |
BXGD002458 |
Pulmonary Fibrosis |
Respiratory Tract Diseases |
| C0034091 |
BXGD002463 |
Pulmonary Veno-Occlusive Disease (disorder) |
Respiratory Tract Diseases; Cardiovascular Diseases |
| C0035126 |
BXGD002509 |
Reperfusion Injury |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0036202 |
BXGD002581 |
Sarcoidosis |
Hemic and Lymphatic Diseases |
| C0036421 |
BXGD002613 |
Systemic Scleroderma |
Skin and Connective Tissue Diseases |
| C0039070 |
BXGD002787 |
Syncope |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0039445 |
BXGD002810 |
Hereditary hemorrhagic telangiectasia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases; Cardiovascular Diseases |
| C0039446 |
BXGD002811 |
Telangiectasis |
Cardiovascular Diseases |
| C0085215 |
BXGD003141 |
Ovarian Failure, Premature |
Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C0085580 |
BXGD003191 |
Essential Hypertension |
Cardiovascular Diseases |
| C0152021 |
BXGD003520 |
Congenital heart disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C0152171 |
BXGD003552 |
Idiopathic pulmonary hypertension |
Respiratory Tract Diseases; Cardiovascular Diseases |
| C0154307 |
BXGD003715 |
Banti's syndrome |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Hemic and Lymphatic Diseases |
| C0162770 |
BXGD003980 |
Right Ventricular Hypertrophy |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0202117 |
BXGD004074 |
Low density lipoprotein cholesterol measurement |
|
| C0205734 |
BXGD004115 |
Diabetes, Autoimmune |
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases |
| C0206081 |
BXGD004152 |
Hyperandrogenism |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases |
| C0220630 |
BXGD004302 |
Adult Liver Carcinoma |
Digestive System Diseases; Neoplasms |
| C0235527 |
BXGD004753 |
Heart Failure, Right-Sided |
Cardiovascular Diseases |
| C0235833 |
BXGD004775 |
Congenital diaphragmatic hernia |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C0242669 |
BXGD005186 |
Placenta, Retained |
Female Urogenital Diseases and Pregnancy Complications |
| C0279000 |
BXGD006622 |
Liver and Intrahepatic Biliary Tract Carcinoma |
Digestive System Diseases; Neoplasms |
| C0279680 |
BXGD006680 |
Transitional cell carcinoma of bladder |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0339510 |
BXGD007257 |
Vitelliform Macular Dystrophy |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C0340100 |
BXGD007304 |
High altitude pulmonary edema |
Respiratory Tract Diseases |
| C0340542 |
BXGD007343 |
Sporadic primary pulmonary hypertension |
Respiratory Tract Diseases |
| C0340543 |
BXGD007344 |
Familial primary pulmonary hypertension |
Respiratory Tract Diseases |
| C0340544 |
BXGD007345 |
Pulmonary arterial hypertension induced by drug |
|
| C0342649 |
BXGD007522 |
Vascular calcification |
Nutritional and Metabolic Diseases |
| C0345893 |
BXGD007743 |
Juvenile polyposis syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms |
| C0345904 |
BXGD007745 |
Malignant neoplasm of liver |
Digestive System Diseases; Neoplasms |
| C0376154 |
BXGD007980 |
Skin callus |
Skin and Connective Tissue Diseases |
| C0376358 |
BXGD007992 |
Malignant neoplasm of prostate |
Neoplasms; Male Urogenital Diseases |
| C0392885 |
BXGD008071 |
High density lipoprotein measurement |
|
| C0427460 |
BXGD008616 |
Red cell distribution width determination |
|
| C0428472 |
BXGD008630 |
Serum HDL cholesterol measurement |
|
| C0520861 |
BXGD009115 |
Raised jugular venous pressure |
|
| C0585442 |
BXGD009593 |
Osteosarcoma of bone |
Neoplasms |
| C0596263 |
BXGD009639 |
Carcinogenesis |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0600139 |
BXGD009695 |
Prostate carcinoma |
Neoplasms; Male Urogenital Diseases |
| C0677932 |
BXGD009736 |
Progressive Neoplastic Disease |
|
| C0678222 |
BXGD009749 |
Breast Carcinoma |
Neoplasms; Skin and Connective Tissue Diseases |
| C0679427 |
BXGD009777 |
myeloblastosis |
Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases |
| C0699790 |
BXGD009866 |
Colon Carcinoma |
Digestive System Diseases; Neoplasms |
| C0700095 |
BXGD009875 |
Central neuroblastoma |
Neoplasms; Nervous System Diseases |
| C0747845 |
BXGD010184 |
early pregnancy |
|
| C0856169 |
BXGD011096 |
Endothelial dysfunction |
|
| C1096458 |
BXGD011622 |
Vascular occlusion |
Cardiovascular Diseases |
| C1150929 |
BXGD011768 |
2-oxo-hept-3-ene-1,7-dioate hydratase activity |
|
| C1257931 |
BXGD011815 |
Mammary Neoplasms, Human |
Neoplasms; Skin and Connective Tissue Diseases |
| C1269955 |
BXGD012005 |
Tumor Cell Invasion |
|
| C1275685 |
BXGD012092 |
Avellino corneal dystrophy |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C1304746 |
BXGD012343 |
RDW - Red blood cell distribution width result |
|
| C1306459 |
BXGD012361 |
Primary malignant neoplasm |
Neoplasms |
| C1332986 |
BXGD012574 |
Childhood Osteosarcoma |
Neoplasms |
| C1445957 |
BXGD013081 |
Serum total cholesterol measurement |
|
| C1458155 |
BXGD013136 |
Mammary Neoplasms |
Neoplasms; Skin and Connective Tissue Diseases |
| C1504382 |
BXGD013140 |
Pulmonary arterial medial hypertrophy |
Respiratory Tract Diseases |
| C1611743 |
BXGD013456 |
Familial (FPAH) |
|
| C1629609 |
BXGD013479 |
Age at menopause |
|
| C1701938 |
BXGD013524 |
Associated Pulmonary Arterial Hypertension |
Respiratory Tract Diseases |
| C1701939 |
BXGD013525 |
Familial pulmonary arterial hypertension |
|
| C1800706 |
BXGD013755 |
Idiopathic Pulmonary Fibrosis |
Respiratory Tract Diseases |
| C1867421 |
BXGD016451 |
Elevated right atrial pressure |
|
| C1867423 |
BXGD016452 |
Increased pulmonary vascular resistance |
|
| C1867424 |
BXGD016453 |
Pulmonary artery vasoconstriction |
|
| C1956346 |
BXGD016627 |
Coronary Artery Disease |
Cardiovascular Diseases |
| C1969342 |
BXGD016771 |
PULMONARY HYPERTENSION, PRIMARY, DEXFENFLURAMINE-ASSOCIATED |
Respiratory Tract Diseases |
| C1969343 |
BXGD016772 |
Pulmonary Hypertension, Primary, Fenfluramine-Associated |
Respiratory Tract Diseases |
| C2363973 |
BXGD017121 |
Chronic thromboembolic pulmonary hypertension |
Respiratory Tract Diseases; Cardiovascular Diseases |
| C2931384 |
BXGD018014 |
Moyamoya disease 1 |
Nervous System Diseases; Cardiovascular Diseases |
| C2939419 |
BXGD018178 |
Secondary Neoplasm |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C2939447 |
BXGD018179 |
Right ventricular failure |
Cardiovascular Diseases |
| C2973725 |
BXGD018205 |
Pulmonary arterial hypertension |
Respiratory Tract Diseases; Cardiovascular Diseases |
| C3203102 |
BXGD018555 |
Idiopathic pulmonary arterial hypertension |
Respiratory Tract Diseases |
| C3278509 |
BXGD018742 |
Spinal fusion |
|
| C3539781 |
BXGD019086 |
Progressive cGVHD |
|
| C3665995 |
BXGD019315 |
Secondary pulmonary arterial hypertension |
|
| C3697119 |
BXGD019352 |
Pulmonary arterial hypertension associated with congenital heart disease |
|
| C3714844 |
BXGD019435 |
Pulmonary Hypertension, Primary, 1, With Hereditary Hemorrhagic Telangiectasia |
Respiratory Tract Diseases |
| C3806932 |
BXGD019527 |
PULMONARY VENOOCCLUSIVE DISEASE 1 |
|
| C3887658 |
BXGD019913 |
PULMONARY VENOOCCLUSIVE DISEASE 1, AUTOSOMAL DOMINANT |
Respiratory Tract Diseases; Cardiovascular Diseases |
| C4023403 |
BXGD021179 |
Arterial intimal fibrosis |
|
| C4025217 |
BXGD021597 |
Pulmonary aterial intimal fibrosis |
|
| C4025731 |
BXGD021763 |
Abnormal thrombosis |
|
| C4086165 |
BXGD022126 |
Childhood Neuroblastoma |
Neoplasms |
| C4280802 |
BXGD022406 |
Pulmonary venous occlusion |
|
| C4527152 |
BXGD023153 |
Tricuspid Valve Regurgitation Velocity |
|
| C4552070 |
BXGD023481 |
Pulmonary Hypertension, Primary, 1 |
Respiratory Tract Diseases |
| C4554601 |
BXGD023566 |
Amyloidosis cutis dyschromia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases |
| C4704874 |
BXGD023682 |
Mammary Carcinoma, Human |
Neoplasms; Skin and Connective Tissue Diseases |