| C0000737 |
BXGD000005 |
Abdominal Pain |
Pathological Conditions, Signs and Symptoms |
| C0001430 |
BXGD000054 |
Adenoma |
Neoplasms |
| C0001948 |
BXGD000091 |
Alcohol consumption |
Behavior and Behavior Mechanisms |
| C0002170 |
BXGD000105 |
Alopecia |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases |
| C0002312 |
BXGD000107 |
alpha-Thalassemia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0002395 |
BXGD000111 |
Alzheimer's Disease |
Nervous System Diseases; Mental Disorders |
| C0002453 |
BXGD000117 |
Amenorrhea |
Pathological Conditions, Signs and Symptoms |
| C0002726 |
BXGD000125 |
Amyloidosis |
Nutritional and Metabolic Diseases |
| C0002736 |
BXGD000127 |
Amyotrophic Lateral Sclerosis |
Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0002871 |
BXGD000132 |
Anemia |
Hemic and Lymphatic Diseases |
| C0002874 |
BXGD000134 |
Aplastic Anemia |
Hemic and Lymphatic Diseases |
| C0002875 |
BXGD000135 |
Cooley's anemia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0002876 |
BXGD000136 |
Congenital dyserythropoietic anemia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0002878 |
BXGD000137 |
Anemia, Hemolytic |
Hemic and Lymphatic Diseases |
| C0002895 |
BXGD000152 |
Anemia, Sickle Cell |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0003467 |
BXGD000194 |
Anxiety |
Behavior and Behavior Mechanisms |
| C0003811 |
BXGD000222 |
Cardiac Arrhythmia |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0003850 |
BXGD000225 |
Arteriosclerosis |
Cardiovascular Diseases |
| C0003862 |
BXGD000230 |
Arthralgia |
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases |
| C0003864 |
BXGD000231 |
Arthritis |
Musculoskeletal Diseases |
| C0003868 |
BXGD000233 |
Arthritis, Gouty |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C0003873 |
BXGD000236 |
Rheumatoid Arthritis |
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases |
| C0003962 |
BXGD000244 |
Ascites |
Pathological Conditions, Signs and Symptoms |
| C0004114 |
BXGD000255 |
Astrocytoma |
Neoplasms |
| C0004153 |
BXGD000260 |
Atherosclerosis |
Cardiovascular Diseases |
| C0004352 |
BXGD000269 |
Autistic Disorder |
Mental Disorders |
| C0004509 |
BXGD000275 |
Azoospermia |
Male Urogenital Diseases |
| C0004763 |
BXGD000289 |
Barrett Esophagus |
Digestive System Diseases; Neoplasms |
| C0004943 |
BXGD000297 |
Behcet Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases |
| C0005283 |
BXGD000308 |
beta Thalassemia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0005612 |
BXGD000317 |
Birth Weight |
Pathological Conditions, Signs and Symptoms |
| C0005823 |
BXGD000339 |
Blood Pressure |
|
| C0006118 |
BXGD000372 |
Brain Neoplasms |
Neoplasms; Nervous System Diseases |
| 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 |
| C0007104 |
BXGD000427 |
Female Breast Carcinoma |
Neoplasms; Skin and Connective Tissue Diseases |
| C0007134 |
BXGD000443 |
Renal Cell Carcinoma |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0007193 |
BXGD000451 |
Cardiomyopathy, Dilated |
Cardiovascular Diseases |
| C0007194 |
BXGD000452 |
Hypertrophic Cardiomyopathy |
Cardiovascular Diseases |
| C0007222 |
BXGD000454 |
Cardiovascular Diseases |
Cardiovascular Diseases |
| C0007570 |
BXGD000467 |
Celiac Disease |
Digestive System Diseases; Nutritional and Metabolic Diseases |
| C0007785 |
BXGD000485 |
Cerebral Infarction |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases |
| C0008074 |
BXGD000519 |
Child Development Disorders, Pervasive |
Mental Disorders |
| C0008370 |
BXGD000534 |
Cholestasis |
Digestive System Diseases |
| C0009088 |
BXGD000585 |
Cluster Headache |
Nervous System Diseases |
| C0009402 |
BXGD000605 |
Colorectal Carcinoma |
Digestive System Diseases; Neoplasms |
| C0009447 |
BXGD000613 |
Common Variable Immunodeficiency |
Immune System Diseases |
| C0009806 |
BXGD000633 |
Constipation |
Pathological Conditions, Signs and Symptoms |
| C0010054 |
BXGD000647 |
Coronary Arteriosclerosis |
Cardiovascular Diseases |
| C0010068 |
BXGD000648 |
Coronary heart disease |
Cardiovascular Diseases |
| C0010346 |
BXGD000664 |
Crohn Disease |
Digestive System Diseases |
| C0010674 |
BXGD000683 |
Cystic Fibrosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Respiratory Tract Diseases |
| C0011265 |
BXGD000708 |
Presenile dementia |
Nervous System Diseases; Mental Disorders |
| C0011269 |
BXGD000710 |
Dementia, Vascular |
Nervous System Diseases; Mental Disorders; Cardiovascular 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 |
| 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 |
| C0011881 |
BXGD000760 |
Diabetic Nephropathy |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases |
| C0011884 |
BXGD000762 |
Diabetic Retinopathy |
Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases |
| C0012715 |
BXGD000783 |
Iron Metabolism Disorders |
Nutritional and Metabolic Diseases |
| C0014173 |
BXGD000903 |
Endometrial Hyperplasia |
Female Urogenital Diseases and Pregnancy Complications |
| C0014772 |
BXGD000948 |
Red Blood Cell Count measurement |
|
| C0015672 |
BXGD001011 |
Fatigue |
Pathological Conditions, Signs and Symptoms |
| C0015695 |
BXGD001013 |
Fatty Liver |
Digestive System Diseases |
| C0015696 |
BXGD001014 |
Fatty Liver, Alcoholic |
Digestive System Diseases; Chemically-Induced Disorders |
| C0015967 |
BXGD001030 |
Fever |
Pathological Conditions, Signs and Symptoms |
| C0016053 |
BXGD001041 |
Fibromyalgia |
Musculoskeletal Diseases; Nervous System Diseases |
| C0016059 |
BXGD001043 |
Fibrosis |
Pathological Conditions, Signs and Symptoms |
| C0016719 |
BXGD001074 |
Friedreich Ataxia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0017178 |
BXGD001102 |
Gastrointestinal Diseases |
Digestive System Diseases |
| C0017205 |
BXGD001105 |
Gaucher Disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0017551 |
BXGD001116 |
Gilbert Disease (disorder) |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0017636 |
BXGD001131 |
Glioblastoma |
Neoplasms |
| C0017638 |
BXGD001132 |
Glioma |
Neoplasms |
| C0018099 |
BXGD001172 |
Gout |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C0018418 |
BXGD001192 |
Gynecomastia |
Skin and Connective Tissue Diseases |
| C0018553 |
BXGD001203 |
Hamartoma Syndrome, Multiple |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms |
| C0018799 |
BXGD001224 |
Heart Diseases |
Cardiovascular Diseases |
| C0018800 |
BXGD001225 |
Cardiomegaly |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0018801 |
BXGD001226 |
Heart failure |
Cardiovascular Diseases |
| C0018802 |
BXGD001227 |
Congestive heart failure |
Cardiovascular Diseases |
| C0018862 |
BXGD001242 |
Heberden node |
Musculoskeletal Diseases |
| C0018935 |
BXGD001252 |
Hematocrit procedure |
|
| C0018939 |
BXGD001253 |
Hematological Disease |
Hemic and Lymphatic Diseases |
| C0018995 |
BXGD001265 |
Hemochromatosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0019045 |
BXGD001269 |
Hemoglobinopathies |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0019069 |
BXGD001277 |
Hemophilia A |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0019114 |
BXGD001287 |
Hemosiderosis |
Nutritional and Metabolic Diseases |
| C0019156 |
BXGD001292 |
Hepatic Veno-Occlusive Disease |
Digestive System Diseases; Cardiovascular Diseases |
| C0019158 |
BXGD001293 |
Hepatitis |
Digestive System Diseases |
| C0019159 |
BXGD001294 |
Hepatitis A |
Digestive System Diseases; Infections |
| C0019163 |
BXGD001295 |
Hepatitis B |
Digestive System Diseases; Infections |
| C0019189 |
BXGD001298 |
Hepatitis, Chronic |
Digestive System Diseases |
| C0019196 |
BXGD001301 |
Hepatitis C |
Digestive System Diseases; Infections |
| C0019202 |
BXGD001302 |
Hepatolenticular Degeneration |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0019209 |
BXGD001305 |
Hepatomegaly |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C0019693 |
BXGD001346 |
HIV Infections |
Infections; Immune System Diseases |
| C0019829 |
BXGD001350 |
Hodgkin Disease |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0020473 |
BXGD001396 |
Hyperlipidemia |
Nutritional and Metabolic Diseases |
| C0020538 |
BXGD001422 |
Hypertensive disease |
Cardiovascular Diseases |
| C0020541 |
BXGD001424 |
Portal Hypertension |
Digestive System Diseases |
| C0020619 |
BXGD001447 |
Hypogonadism |
Endocrine System Diseases |
| C0021364 |
BXGD001500 |
Male infertility |
Male Urogenital Diseases |
| C0021390 |
BXGD001503 |
Inflammatory Bowel Diseases |
Digestive System Diseases |
| C0021704 |
BXGD001510 |
Intelligence |
Behavior and Behavior Mechanisms |
| C0022387 |
BXGD001543 |
Jervell-Lange Nielsen Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C0022408 |
BXGD001544 |
Arthropathy |
Musculoskeletal Diseases |
| C0022658 |
BXGD001570 |
Kidney Diseases |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0022661 |
BXGD001572 |
Kidney Failure, Chronic |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0023176 |
BXGD001612 |
Lead Poisoning |
Chemically-Induced Disorders |
| C0023380 |
BXGD001640 |
Lethargy |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms |
| C0023418 |
BXGD001642 |
leukemia |
Neoplasms |
| C0023449 |
BXGD001650 |
Acute lymphocytic leukemia |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0023452 |
BXGD001651 |
Childhood Acute Lymphoblastic Leukemia |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0023467 |
BXGD001658 |
Leukemia, Myelocytic, Acute |
Neoplasms |
| C0023487 |
BXGD001669 |
Acute Promyelocytic Leukemia |
Neoplasms |
| C0023508 |
BXGD001675 |
White Blood Cell Count procedure |
|
| C0023787 |
BXGD001698 |
Lipodystrophy |
Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases |
| C0023890 |
BXGD001713 |
Liver Cirrhosis |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C0023891 |
BXGD001714 |
Liver Cirrhosis, Alcoholic |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Chemically-Induced Disorders |
| C0023895 |
BXGD001717 |
Liver diseases |
Digestive System Diseases |
| C0023896 |
BXGD001718 |
Alcoholic Liver Diseases |
Digestive System Diseases; Chemically-Induced Disorders |
| C0023903 |
BXGD001720 |
Liver neoplasms |
Digestive System Diseases; Neoplasms |
| C0023976 |
BXGD001724 |
Long QT Syndrome |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C0024115 |
BXGD001732 |
Lung diseases |
Respiratory Tract Diseases |
| C0024299 |
BXGD001758 |
Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0024623 |
BXGD001791 |
Malignant neoplasm of stomach |
Digestive System Diseases; Neoplasms |
| C0025286 |
BXGD001850 |
Meningioma |
Neoplasms; Nervous System Diseases |
| C0026764 |
BXGD001928 |
Multiple Myeloma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases |
| C0026769 |
BXGD001930 |
Multiple Sclerosis |
Immune System Diseases; Nervous System Diseases |
| C0026985 |
BXGD001956 |
Myelodysplasia |
|
| C0027051 |
BXGD001963 |
Myocardial Infarction |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0027651 |
BXGD002009 |
Neoplasms |
Neoplasms |
| C0027672 |
BXGD002020 |
Neoplastic Syndromes, Hereditary |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms |
| C0027819 |
BXGD002043 |
Neuroblastoma |
Neoplasms |
| C0028754 |
BXGD002082 |
Obesity |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases |
| C0029408 |
BXGD002137 |
Degenerative polyarthritis |
Musculoskeletal Diseases |
| C0029410 |
BXGD002138 |
Osteoarthritis of hip |
Musculoskeletal Diseases |
| C0029453 |
BXGD002154 |
Osteopenia |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C0029456 |
BXGD002157 |
Osteoporosis |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C0030567 |
BXGD002240 |
Parkinson Disease |
Nervous System Diseases |
| C0031117 |
BXGD002285 |
Peripheral Neuropathy |
Nervous System Diseases |
| C0032181 |
BXGD002332 |
Platelet Count measurement |
|
| C0032227 |
BXGD002336 |
Pleural effusion disorder |
Respiratory Tract Diseases |
| C0032463 |
BXGD002357 |
Polycythemia Vera |
Neoplasms; Hemic and Lymphatic Diseases |
| C0032584 |
BXGD002363 |
polyps |
Pathological Conditions, Signs and Symptoms |
| C0032708 |
BXGD002368 |
Disorders of Porphyrin Metabolism |
Nutritional and Metabolic Diseases |
| C0033802 |
BXGD002425 |
Pseudogout |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C0033975 |
BXGD002447 |
Psychotic Disorders |
Mental Disorders |
| C0035258 |
BXGD002523 |
Restless Legs Syndrome |
Nervous System Diseases; Mental Disorders |
| C0035309 |
BXGD002530 |
Retinal Diseases |
Eye Diseases |
| C0035435 |
BXGD002549 |
Rheumatism |
Skin and Connective Tissue Diseases; Musculoskeletal Diseases |
| C0036202 |
BXGD002581 |
Sarcoidosis |
Hemic and Lymphatic Diseases |
| C0036337 |
BXGD002598 |
Schizoaffective Disorder |
Mental Disorders |
| C0036341 |
BXGD002600 |
Schizophrenia |
Mental Disorders |
| C0036421 |
BXGD002613 |
Systemic Scleroderma |
Skin and Connective Tissue Diseases |
| C0037054 |
BXGD002663 |
Sickle Cell Trait |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0037061 |
BXGD002664 |
Siderosis |
Respiratory Tract Diseases; Occupational Diseases |
| C0037284 |
BXGD002679 |
Skin lesion |
Skin and Connective Tissue Diseases |
| C0037889 |
BXGD002709 |
Hereditary spherocytosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0038002 |
BXGD002723 |
Splenomegaly |
Pathological Conditions, Signs and Symptoms |
| C0038454 |
BXGD002760 |
Cerebrovascular accident |
Nervous System Diseases; Cardiovascular Diseases |
| C0039231 |
BXGD002799 |
Tachycardia |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0039446 |
BXGD002811 |
Telangiectasis |
Cardiovascular Diseases |
| C0039730 |
BXGD002826 |
Thalassemia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0040028 |
BXGD002835 |
Thrombocythemia, Essential |
Hemic and Lymphatic Diseases |
| C0040128 |
BXGD002844 |
Thyroid Diseases |
Endocrine System Diseases |
| C0042344 |
BXGD002976 |
Varicose Ulcer |
Skin and Connective Tissue Diseases; Cardiovascular Diseases |
| C0042345 |
BXGD002977 |
Varicosity |
Cardiovascular Diseases |
| C0042571 |
BXGD002991 |
Vertigo |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases |
| C0042769 |
BXGD002999 |
Virus Diseases |
Infections |
| C0042963 |
BXGD003018 |
Vomiting |
Pathological Conditions, Signs and Symptoms |
| C0085207 |
BXGD003140 |
Gestational Diabetes |
Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C0085400 |
BXGD003165 |
Neurofibrillary degeneration (morphologic abnormality) |
|
| C0085576 |
BXGD003188 |
Iron-Refractory Iron Deficiency Anemia |
Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases |
| C0085578 |
BXGD003190 |
Thalassemia Minor |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0085580 |
BXGD003191 |
Essential Hypertension |
Cardiovascular Diseases |
| C0085661 |
BXGD003229 |
Onycholysis |
Skin and Connective Tissue Diseases |
| C0085669 |
BXGD003233 |
Acute leukemia |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0085762 |
BXGD003251 |
Alcohol abuse |
Chemically-Induced Disorders; Mental Disorders |
| C0149521 |
BXGD003328 |
Pancreatitis, Chronic |
Digestive System Diseases |
| C0149931 |
BXGD003388 |
Migraine Disorders |
Nervous System Diseases |
| C0150055 |
BXGD003401 |
Chronic pain |
Pathological Conditions, Signs and Symptoms |
| C0151744 |
BXGD003469 |
Myocardial Ischemia |
Cardiovascular Diseases |
| C0151861 |
BXGD003491 |
Porphyruria |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases |
| C0151900 |
BXGD003500 |
Serum iron raised |
Nutritional and Metabolic Diseases |
| C0155626 |
BXGD003806 |
Acute myocardial infarction |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0156312 |
BXGD003849 |
Atrophy of testis |
Male Urogenital Diseases; Endocrine System Diseases |
| C0162309 |
BXGD003934 |
Adrenoleukodystrophy |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Endocrine System Diseases |
| C0162316 |
BXGD003936 |
Iron deficiency anemia |
Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases |
| C0162532 |
BXGD003951 |
Variegate Porphyria |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases |
| C0162539 |
BXGD003955 |
IgG Deficiency disorder |
Immune System Diseases; Hemic and Lymphatic Diseases |
| C0162566 |
BXGD003958 |
Porphyria Cutanea Tarda |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases |
| C0162834 |
BXGD003988 |
Hyperpigmentation |
Skin and Connective Tissue Diseases |
| C0202105 |
BXGD004072 |
Transferrin measurement |
|
| C0202117 |
BXGD004074 |
Low density lipoprotein cholesterol measurement |
|
| C0206161 |
BXGD004167 |
Reticulocyte count (procedure) |
|
| C0220597 |
BXGD004292 |
Adult Hodgkin Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0220630 |
BXGD004302 |
Adult Liver Carcinoma |
Digestive System Diseases; Neoplasms |
| C0220644 |
BXGD004306 |
Childhood Hodgkin Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0221757 |
BXGD004472 |
alpha 1-Antitrypsin Deficiency |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Respiratory Tract Diseases |
| C0235653 |
BXGD004762 |
Malignant neoplasm of female breast |
Neoplasms; Skin and Connective Tissue Diseases |
| C0235946 |
BXGD004789 |
Cerebral atrophy |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0235974 |
BXGD004796 |
Pancreatic carcinoma |
Digestive System Diseases; Neoplasms; Endocrine System Diseases |
| C0238033 |
BXGD004861 |
Carcinoma of Male Breast |
Neoplasms; Skin and Connective Tissue Diseases |
| C0238158 |
BXGD004887 |
Secondary hemochromatosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0239946 |
BXGD005010 |
Fibrosis, Liver |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C0240066 |
BXGD005016 |
Iron deficiency |
Nutritional and Metabolic Diseases |
| C0241013 |
BXGD005075 |
Increased serum ferritin |
|
| C0241181 |
BXGD005084 |
Fragile skin |
|
| C0242350 |
BXGD005154 |
Erectile dysfunction |
Male Urogenital Diseases; Mental Disorders |
| C0242422 |
BXGD005163 |
Parkinsonian Disorders |
Nervous System Diseases |
| C0242787 |
BXGD005195 |
Malignant neoplasm of male breast |
Neoplasms; Skin and Connective Tissue Diseases; Endocrine System Diseases |
| C0263746 |
BXGD005346 |
Osteoarthritis of the hand |
Musculoskeletal Diseases |
| C0265219 |
BXGD005468 |
Miller Dieker syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0267795 |
BXGD005776 |
Subacute hepatic necrosis |
Digestive System Diseases |
| C0267809 |
BXGD005779 |
Cirrhosis, Cryptogenic |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C0267963 |
BXGD005796 |
Exocrine pancreatic insufficiency |
Digestive System Diseases |
| C0268059 |
BXGD005805 |
Neonatal hemochromatosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0268060 |
BXGD005806 |
Juvenile hemochromatosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0268323 |
BXGD005897 |
Familial porphyria cutanea tarda |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases |
| C0271623 |
BXGD006222 |
Hypogonadotropic hypogonadism |
Endocrine System Diseases |
| C0271650 |
BXGD006227 |
Impaired glucose tolerance |
Nutritional and Metabolic Diseases |
| C0271979 |
BXGD006283 |
Thalassemia Intermedia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0272024 |
BXGD006295 |
Secondary acquired sideroblastic anemia |
Hemic and Lymphatic Diseases |
| C0276496 |
BXGD006426 |
Familial Alzheimer Disease (FAD) |
Nervous System Diseases; Mental Disorders |
| C0276623 |
BXGD006433 |
Chronic viral hepatitis |
Digestive System Diseases |
| C0279000 |
BXGD006622 |
Liver and Intrahepatic Biliary Tract Carcinoma |
Digestive System Diseases; Neoplasms |
| C0279702 |
BXGD006685 |
Conventional (Clear Cell) Renal Cell Carcinoma |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0281361 |
BXGD006774 |
Adenocarcinoma of pancreas |
Digestive System Diseases; Neoplasms; Endocrine System Diseases |
| C0282193 |
BXGD006798 |
Iron Overload |
Nutritional and Metabolic Diseases |
| C0302332 |
BXGD006841 |
Poisoning syndrome |
|
| C0302486 |
BXGD006847 |
Erythrophagocytosis |
|
| C0333293 |
BXGD006942 |
Healing ulcer |
Pathological Conditions, Signs and Symptoms |
| C0337439 |
BXGD007160 |
Iron measurement |
|
| C0338656 |
BXGD007211 |
Impaired cognition |
Mental Disorders |
| C0341299 |
BXGD007399 |
Collagenous Sprue |
Digestive System Diseases; Nutritional and Metabolic Diseases |
| C0341439 |
BXGD007408 |
Chronic liver disease |
Digestive System Diseases |
| C0342257 |
BXGD007447 |
Complications of Diabetes Mellitus |
Endocrine System Diseases |
| C0342637 |
BXGD007517 |
Hypocalciuric hypercalcemia, familial, type 1 |
Nutritional and Metabolic Diseases |
| C0342784 |
BXGD007551 |
Pearson's marrow-pancreas syndrome |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0342886 |
BXGD007576 |
Primary hypertriglyceridemia |
Nutritional and Metabolic Diseases |
| C0345904 |
BXGD007745 |
Malignant neoplasm of liver |
Digestive System Diseases; Neoplasms |
| C0346647 |
BXGD007832 |
Malignant neoplasm of pancreas |
Digestive System Diseases; Neoplasms; Endocrine System Diseases |
| C0349506 |
BXGD007912 |
Photosensitivity of skin |
Skin and Connective Tissue Diseases |
| C0369183 |
BXGD007960 |
Erythrocyte Mean Corpuscular Hemoglobin Test |
|
| C0373607 |
BXGD007962 |
Ferritin measurement |
|
| C0374997 |
BXGD007967 |
Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site |
|
| C0376358 |
BXGD007992 |
Malignant neoplasm of prostate |
Neoplasms; Male Urogenital Diseases |
| C0376545 |
BXGD008002 |
Hematologic Neoplasms |
Neoplasms; Hemic and Lymphatic Diseases |
| C0392514 |
BXGD008051 |
Hereditary hemochromatosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0400966 |
BXGD008266 |
Non-alcoholic Fatty Liver Disease |
Digestive System Diseases |
| C0403447 |
BXGD008285 |
Chronic Kidney Insufficiency |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0409952 |
BXGD008399 |
Idiopathic osteoarthritis |
Musculoskeletal Diseases |
| C0409959 |
BXGD008400 |
Osteoarthritis, Knee |
Musculoskeletal Diseases |
| C0424295 |
BXGD008524 |
Hyperactive behavior |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0427460 |
BXGD008616 |
Red cell distribution width determination |
|
| C0428474 |
BXGD008631 |
Serum LDL cholesterol measurement |
|
| C0428545 |
BXGD008632 |
Serum transferrin measurement |
|
| C0428578 |
BXGD008634 |
Iron level result |
|
| C0428883 |
BXGD008639 |
Diastolic blood pressure |
|
| C0428886 |
BXGD008640 |
Mean blood pressure |
|
| C0442874 |
BXGD008814 |
Neuropathy |
Nervous System Diseases |
| C0474535 |
BXGD008954 |
Mean corpuscular hemoglobin concentration determination |
|
| C0476089 |
BXGD008977 |
Endometrial Carcinoma |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications |
| C0494463 |
BXGD009029 |
Alzheimer Disease, Late Onset |
Nervous System Diseases; Mental Disorders |
| C0497327 |
BXGD009061 |
Dementia |
Nervous System Diseases; Mental Disorders |
| C0518015 |
BXGD009068 |
Hemoglobin measurement |
|
| C0520463 |
BXGD009085 |
Chronic active hepatitis |
Digestive System Diseases |
| C0522224 |
BXGD009198 |
Paralysed |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0524587 |
BXGD009232 |
Mean Corpuscular Volume (result) |
|
| C0524620 |
BXGD009236 |
Metabolic Syndrome X |
Nutritional and Metabolic Diseases |
| C0524851 |
BXGD009246 |
Neurodegenerative Disorders |
Nervous System Diseases |
| C0524909 |
BXGD009247 |
Hepatitis B, Chronic |
Digestive System Diseases; Infections |
| C0524910 |
BXGD009248 |
Hepatitis C, Chronic |
Digestive System Diseases; Infections |
| C0524988 |
BXGD009253 |
Schnitzler Syndrome |
Immune System Diseases |
| C0546126 |
BXGD009328 |
Acute Confusional Senile Dementia |
Nervous System Diseases; Mental Disorders |
| C0553730 |
BXGD009417 |
Calcium pyrophosphate deposition disease |
Musculoskeletal Diseases |
| C0577631 |
BXGD009535 |
Carotid Atherosclerosis |
Nervous System Diseases; Cardiovascular Diseases |
| C0581384 |
BXGD009568 |
Chronic anemia |
Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases |
| C0584960 |
BXGD009579 |
Factor V Leiden mutation |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0596263 |
BXGD009639 |
Carcinogenesis |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0600139 |
BXGD009695 |
Prostate carcinoma |
Neoplasms; Male Urogenital Diseases |
| C0677886 |
BXGD009734 |
Epithelial ovarian cancer |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C0678222 |
BXGD009749 |
Breast Carcinoma |
Neoplasms; Skin and Connective Tissue Diseases |
| C0687132 |
BXGD009839 |
heavy drinking |
|
| C0696113 |
BXGD009857 |
Serum ferritin measurement |
|
| C0699790 |
BXGD009866 |
Colon Carcinoma |
Digestive System Diseases; Neoplasms |
| C0699791 |
BXGD009867 |
Stomach Carcinoma |
Digestive System Diseases; Neoplasms |
| C0700095 |
BXGD009875 |
Central neuroblastoma |
Neoplasms; Nervous System Diseases |
| C0700379 |
BXGD009890 |
Total iron binding capacity function |
|
| C0740394 |
BXGD009989 |
Hyperuricemia |
Pathological Conditions, Signs and Symptoms |
| C0741237 |
BXGD010027 |
arthritis symptoms |
|
| C0745744 |
BXGD010133 |
End Stage Liver Disease |
Digestive System Diseases |
| C0750900 |
BXGD010241 |
Alzheimer's Disease, Focal Onset |
Nervous System Diseases; Mental Disorders |
| C0750901 |
BXGD010242 |
Alzheimer Disease, Early Onset |
Nervous System Diseases; Mental Disorders |
| C0751072 |
BXGD010312 |
Frontotemporal Lobar Degeneration |
Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders |
| C0751606 |
BXGD010523 |
Adult Acute Lymphocytic Leukemia |
|
| C0751955 |
BXGD010652 |
Brain Infarction |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases |
| C0850666 |
BXGD010901 |
Infection caused by Helicobacter pylori |
Infections |
| C0865274 |
BXGD011284 |
High-oxygen-affinity hemoglobin |
|
| C0869532 |
BXGD011308 |
Beta thalassemia minor |
|
| C0871470 |
BXGD011316 |
Systolic Pressure |
|
| C0872084 |
BXGD011319 |
Sarcopenia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0878521 |
BXGD011367 |
Beta thalassemia trait |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0878544 |
BXGD011368 |
Cardiomyopathies |
Cardiovascular Diseases |
| C0878682 |
BXGD011388 |
Ceruloplasmin deficiency |
Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0948008 |
BXGD011499 |
Ischemic stroke |
Nervous System Diseases; Cardiovascular Diseases |
| C0948120 |
BXGD011507 |
Hepatic siderosis |
Nutritional and Metabolic Diseases |
| C0948441 |
BXGD011538 |
Venoocclusive disease |
Cardiovascular Diseases |
| C0949059 |
BXGD011568 |
Polyp of large intestine |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Neoplasms |
| C0949690 |
BXGD011584 |
Spondylarthritis |
Musculoskeletal Diseases |
| C1141933 |
BXGD011725 |
Multi-organ disorder |
|
| C1168443 |
BXGD011794 |
Pseudocholinesterase Measurement |
|
| C1261502 |
BXGD011856 |
Finding of Mean Corpuscular Hemoglobin |
|
| C1262289 |
BXGD011878 |
Dysmetabolic syndrome |
|
| C1263846 |
BXGD011897 |
Attention deficit hyperactivity disorder |
Mental Disorders |
| C1269955 |
BXGD012005 |
Tumor Cell Invasion |
|
| C1270972 |
BXGD012006 |
Mild cognitive disorder |
Mental Disorders |
| C1276127 |
BXGD012106 |
Sporadic porphyria cutanea tarda |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases |
| C1277709 |
BXGD012113 |
Transferrin saturation measurement |
|
| C1280433 |
BXGD012125 |
Lipoatrophy |
Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases |
| C1283048 |
BXGD012160 |
Iron binding capacity total measurement |
|
| C1292778 |
BXGD012237 |
Chronic myeloproliferative disorder |
Neoplasms; Hemic and Lymphatic Diseases |
| C1302401 |
BXGD012303 |
Adenoma of large intestine |
Digestive System Diseases; Neoplasms |
| C1304746 |
BXGD012343 |
RDW - Red blood cell distribution width result |
|
| C1305849 |
BXGD012347 |
Diastolic blood pressure measurement |
|
| C1306459 |
BXGD012361 |
Primary malignant neoplasm |
Neoplasms |
| C1306620 |
BXGD012371 |
Systolic blood pressure measurement |
|
| C1318312 |
BXGD012392 |
Serum iron measurement |
|
| C1332206 |
BXGD012504 |
Adult Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C1332977 |
BXGD012569 |
Childhood Leukemia |
Neoplasms |
| C1332979 |
BXGD012571 |
Childhood Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C1333990 |
BXGD012670 |
Hereditary Nonpolyposis Colorectal Cancer |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Nutritional and Metabolic Diseases |
| C1384584 |
BXGD012943 |
Generalized osteoarthritis |
Musculoskeletal Diseases |
| C1445957 |
BXGD013081 |
Serum total cholesterol measurement |
|
| C1449563 |
BXGD013086 |
Cardiomyopathy, Familial Idiopathic |
Cardiovascular Diseases |
| C1456873 |
BXGD013129 |
alpha^+^ Thalassemia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C1458155 |
BXGD013136 |
Mammary Neoplasms |
Neoplasms; Skin and Connective Tissue Diseases |
| C1510586 |
BXGD013176 |
Autism Spectrum Disorders |
Mental Disorders |
| C1561643 |
BXGD013363 |
Chronic Kidney Diseases |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C1611743 |
BXGD013456 |
Familial (FPAH) |
|
| C1621958 |
BXGD013468 |
Glioblastoma Multiforme |
Neoplasms |
| C1623038 |
BXGD013475 |
Cirrhosis |
Pathological Conditions, Signs and Symptoms |
| C1800706 |
BXGD013755 |
Idiopathic Pulmonary Fibrosis |
Respiratory Tract Diseases |
| C1835121 |
BXGD014013 |
Premature osteoarthritis |
Musculoskeletal Diseases |
| C1848701 |
BXGD014967 |
Elevated hepatic transaminase |
|
| C1851400 |
BXGD015210 |
Facial Hypertrichosis |
Skin and Connective Tissue Diseases |
| C1853733 |
BXGD015355 |
HEMOCHROMATOSIS, TYPE 4 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C1856170 |
BXGD015582 |
ALZHEIMER DISEASE, SUSCEPTIBILITY TO |
|
| C1856689 |
BXGD015630 |
FRIEDREICH ATAXIA 1 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C1857108 |
BXGD015677 |
Limitation of joint mobility |
|
| C1857231 |
BXGD015685 |
LACTASE PERSISTENCE |
|
| C1858664 |
BXGD015815 |
HEMOCHROMATOSIS, TYPE 3 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C1861172 |
BXGD016016 |
Venous Thromboembolism |
Cardiovascular Diseases |
| C1861453 |
BXGD016049 |
Pseudohyperkalemia Cardiff |
Nutritional and Metabolic Diseases |
| C1862941 |
BXGD016145 |
Amyotrophic Lateral Sclerosis, Sporadic |
Nutritional and Metabolic Diseases; Nervous System Diseases |
| C1865903 |
BXGD016353 |
Long-tract signs |
|
| C1956346 |
BXGD016627 |
Coronary Artery Disease |
Cardiovascular Diseases |
| C1961102 |
BXGD016673 |
Precursor Cell Lymphoblastic Leukemia Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C1961835 |
BXGD016676 |
Gaucher Disease, Type 1 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C1962966 |
BXGD016678 |
Retinopathy, CTCAE |
|
| C2239101 |
BXGD016963 |
Hemoglobin, CTCAE |
|
| C2239176 |
BXGD016965 |
Liver carcinoma |
Digestive System Diseases; Neoplasms |
| C2316810 |
BXGD017030 |
Chronic kidney disease stage 5 |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C2347761 |
BXGD017049 |
Childhood Myelodysplastic Syndrome |
Hemic and Lymphatic Diseases |
| C2362324 |
BXGD017091 |
Pediatric Obesity |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases |
| C2363741 |
BXGD017100 |
HIV-1 infection |
|
| C2673517 |
BXGD017207 |
PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO |
|
| C2673518 |
BXGD017208 |
PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO |
|
| C2673520 |
BXGD017209 |
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding) |
|
| C2711227 |
BXGD017478 |
Steatohepatitis |
Digestive System Diseases |
| C2713368 |
BXGD017496 |
Hematopoetic Myelodysplasia |
Hemic and Lymphatic Diseases |
| C2827503 |
BXGD017799 |
HFE-Associated Hereditary Hemochromatosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C2931689 |
BXGD018049 |
Dystrophia myotonica 2 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases |
| C2936664 |
BXGD018125 |
Acquired Hypogammaglobulinemia |
Immune System Diseases |
| C2936913 |
BXGD018151 |
Porphyria, South African type |
|
| C2939175 |
BXGD018175 |
Meconium ileus |
Digestive System Diseases |
| C3150862 |
BXGD018343 |
HEMOCHROMATOSIS, JUVENILE, DIGENIC |
|
| C3160718 |
BXGD018468 |
PARKINSON DISEASE, LATE-ONSET |
|
| C3161174 |
BXGD018505 |
Hemoglobin H Disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C3241937 |
BXGD018578 |
Nonalcoholic Steatohepatitis |
Digestive System Diseases |
| C3250443 |
BXGD018584 |
MYOTONIC DYSTROPHY 1 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases |
| C3266262 |
BXGD018600 |
Multiple Chronic Conditions |
Pathological Conditions, Signs and Symptoms |
| C3266753 |
BXGD018603 |
Severe left ventricular systolic dysfunction |
|
| C3280096 |
BXGD018801 |
TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2 |
|
| C3463824 |
BXGD018899 |
MYELODYSPLASTIC SYNDROME |
Hemic and Lymphatic Diseases |
| C3469186 |
BXGD018909 |
HEMOCHROMATOSIS, TYPE 1 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C3495559 |
BXGD018994 |
Juvenile arthritis |
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases |
| C3714514 |
BXGD019409 |
Infection |
Infections |
| C3805877 |
BXGD019492 |
Hyperpigmentation in sun-exposed areas |
Skin and Connective Tissue Diseases |
| C3839044 |
BXGD019766 |
Compensated liver disease |
Digestive System Diseases |
| C3841475 |
BXGD019800 |
beta^+^ Thalassemia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C3854222 |
BXGD019826 |
Human immunodeficiency virus (HIV) II infection category B1 |
|
| C3854388 |
BXGD019830 |
Hyperferritinaemia |
Nutritional and Metabolic Diseases |
| C3872662 |
BXGD019849 |
Chronic active hepatitis C |
Digestive System Diseases; Infections |
| C3900098 |
BXGD020106 |
Adult Myelodysplastic Syndrome |
Hemic and Lymphatic Diseases |
| C4025819 |
BXGD021808 |
Abnormality of the hypothalamus-pituitary axis |
|
| C4025886 |
BXGD021846 |
Severe periodontitis |
Stomatognathic Diseases |
| C4082974 |
BXGD022099 |
Dupuytren's Disease |
Neoplasms; Skin and Connective Tissue Diseases; Musculoskeletal Diseases |
| C4086152 |
BXGD022123 |
Childhood Astrocytoma |
Neoplasms |
| C4086165 |
BXGD022126 |
Childhood Neuroblastoma |
Neoplasms |
| C4528257 |
BXGD023159 |
Corpuscular Hemoglobin Concentration Mean |
|
| C4529962 |
BXGD023178 |
Fatty Liver Disease |
|
| C4551511 |
BXGD023330 |
X-linked sideroblastic anemia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C4551584 |
BXGD023362 |
Brain atrophy |
Nervous System Diseases |
| C4551590 |
BXGD023363 |
Familial renal hypouricemia |
|
| C4552187 |
BXGD023493 |
Cardiac iron overload |
Nutritional and Metabolic Diseases; Cardiovascular Diseases |
| C4703620 |
BXGD023665 |
Decreased level of GABA in serum |
|
| C4721453 |
BXGD023744 |
Peripheral Nervous System Diseases |
Nervous System Diseases |
| C4721610 |
BXGD023760 |
Carcinoma, Ovarian Epithelial |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C4722085 |
BXGD023788 |
Malignant neoplasm of colon and/or rectum |
|
