| C0000737 |
BXGD000005 |
Abdominal Pain |
Pathological Conditions, Signs and Symptoms |
| C0000744 |
BXGD000006 |
Abetalipoproteinemia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0000786 |
BXGD000010 |
Spontaneous abortion |
Female Urogenital Diseases and Pregnancy Complications |
| C0000822 |
BXGD000012 |
Abortion, Tubal |
Female Urogenital Diseases and Pregnancy Complications |
| C0001206 |
BXGD000033 |
Acromegaly |
Musculoskeletal Diseases; Nervous System Diseases; Endocrine System Diseases |
| C0001339 |
BXGD000041 |
Acute pancreatitis |
Digestive System Diseases |
| C0001418 |
BXGD000050 |
Adenocarcinoma |
Neoplasms |
| C0001546 |
BXGD000060 |
Adjustment Disorders |
Mental Disorders |
| C0001815 |
BXGD000078 |
Primary Myelofibrosis |
Hemic and Lymphatic Diseases |
| C0002395 |
BXGD000111 |
Alzheimer's Disease |
Nervous System Diseases; Mental Disorders |
| C0002871 |
BXGD000132 |
Anemia |
Hemic and Lymphatic Diseases |
| C0002873 |
BXGD000133 |
Anemia of chronic disease |
Hemic and Lymphatic Diseases |
| C0002890 |
BXGD000147 |
Leukoerythroblastic Anemia |
Hemic and Lymphatic Diseases |
| C0002893 |
BXGD000150 |
Refractory anemias |
Hemic and Lymphatic Diseases |
| C0002896 |
BXGD000153 |
Sideroblastic anemia |
Hemic and Lymphatic Diseases |
| C0002962 |
BXGD000160 |
Angina Pectoris |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0003123 |
BXGD000178 |
Anorexia |
Pathological Conditions, Signs and Symptoms |
| C0003130 |
BXGD000183 |
Anoxia |
Pathological Conditions, Signs and Symptoms |
| C0003467 |
BXGD000194 |
Anxiety |
Behavior and Behavior Mechanisms |
| C0003469 |
BXGD000195 |
Anxiety Disorders |
Mental Disorders |
| C0003834 |
BXGD000223 |
Arterial insufficiency |
Cardiovascular Diseases |
| C0003850 |
BXGD000225 |
Arteriosclerosis |
Cardiovascular Diseases |
| C0003862 |
BXGD000230 |
Arthralgia |
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases |
| C0003864 |
BXGD000231 |
Arthritis |
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 |
| C0004364 |
BXGD000270 |
Autoimmune Diseases |
Immune System Diseases |
| C0004943 |
BXGD000297 |
Behcet Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases |
| C0005122 |
BXGD000303 |
Beriberi |
Nutritional and Metabolic Diseases |
| C0005684 |
BXGD000319 |
Malignant neoplasm of urinary bladder |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0005695 |
BXGD000323 |
Bladder Neoplasm |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0005699 |
BXGD000325 |
Blast Phase |
Pathological Conditions, Signs and Symptoms; Neoplasms; Hemic and Lymphatic Diseases |
| C0005779 |
BXGD000336 |
Blood Coagulation Disorders |
Hemic and Lymphatic Diseases |
| C0005890 |
BXGD000345 |
Body Height |
|
| C0005940 |
BXGD000352 |
Bone Diseases |
Musculoskeletal Diseases |
| C0006118 |
BXGD000372 |
Brain Neoplasms |
Neoplasms; Nervous System Diseases |
| C0006142 |
BXGD000374 |
Malignant neoplasm of breast |
Neoplasms; Skin and Connective Tissue Diseases |
| C0006413 |
BXGD000397 |
Burkitt Lymphoma |
Neoplasms; Infections; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0006625 |
BXGD000401 |
Cachexia |
Pathological Conditions, Signs and Symptoms |
| C0006663 |
BXGD000403 |
Calcinosis |
Nutritional and Metabolic Diseases |
| C0006826 |
BXGD000408 |
Malignant Neoplasms |
Neoplasms |
| C0007097 |
BXGD000424 |
Carcinoma |
Neoplasms |
| C0007102 |
BXGD000425 |
Malignant tumor of colon |
Digestive System Diseases; Neoplasms |
| C0007131 |
BXGD000441 |
Non-Small Cell Lung Carcinoma |
Neoplasms; Respiratory Tract Diseases |
| C0007134 |
BXGD000443 |
Renal Cell Carcinoma |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0007137 |
BXGD000445 |
Squamous cell carcinoma |
Neoplasms |
| C0007222 |
BXGD000454 |
Cardiovascular Diseases |
Cardiovascular Diseases |
| C0007785 |
BXGD000485 |
Cerebral Infarction |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases |
| C0007787 |
BXGD000487 |
Transient Ischemic Attack |
Nervous System Diseases; Cardiovascular Diseases |
| C0007847 |
BXGD000492 |
Malignant tumor of cervix |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications |
| C0007873 |
BXGD000500 |
Uterine Cervical Neoplasm |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications |
| C0008031 |
BXGD000511 |
Chest Pain |
Pathological Conditions, Signs and Symptoms |
| C0008312 |
BXGD000527 |
Primary biliary cirrhosis |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C0008325 |
BXGD000529 |
Cholecystitis |
Digestive System Diseases |
| C0008497 |
BXGD000549 |
Choriocarcinoma |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications |
| C0008626 |
BXGD000559 |
Congenital chromosomal disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C0009241 |
BXGD000595 |
Cognition Disorders |
Mental Disorders |
| C0009324 |
BXGD000597 |
Ulcerative Colitis |
Digestive System Diseases |
| C0009375 |
BXGD000602 |
Colonic Neoplasms |
Digestive System Diseases; Neoplasms |
| C0009402 |
BXGD000605 |
Colorectal Carcinoma |
Digestive System Diseases; Neoplasms |
| C0009782 |
BXGD000631 |
Connective Tissue Diseases |
Skin and Connective Tissue Diseases |
| C0009812 |
BXGD000634 |
Constitutional Symptom |
|
| C0010054 |
BXGD000647 |
Coronary Arteriosclerosis |
Cardiovascular Diseases |
| C0010068 |
BXGD000648 |
Coronary heart disease |
Cardiovascular Diseases |
| C0010346 |
BXGD000664 |
Crohn Disease |
Digestive System Diseases |
| C0011127 |
BXGD000699 |
Pressure Ulcer |
Skin and Connective Tissue Diseases |
| C0011269 |
BXGD000710 |
Dementia, Vascular |
Nervous System Diseases; Mental Disorders; Cardiovascular Diseases |
| C0011570 |
BXGD000729 |
Mental Depression |
Behavior and Behavior Mechanisms |
| C0011581 |
BXGD000733 |
Depressive disorder |
Mental Disorders |
| C0011603 |
BXGD000734 |
Dermatitis |
Skin and Connective Tissue Diseases |
| C0011615 |
BXGD000738 |
Dermatitis, Atopic |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System 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 |
| C0013080 |
BXGD000797 |
Down Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0013362 |
BXGD000817 |
Dysarthria |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0013491 |
BXGD000847 |
Ecchymosis |
Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases |
| C0013595 |
BXGD000858 |
Eczema |
Skin and Connective Tissue Diseases |
| C0014060 |
BXGD000882 |
Encephalitis, St. Louis |
Infections; Nervous System Diseases |
| C0014122 |
BXGD000896 |
Subacute Bacterial Endocarditis |
Infections; Cardiovascular Diseases |
| C0014457 |
BXGD000915 |
Eosinophilia |
Hemic and Lymphatic Diseases |
| C0014458 |
BXGD000916 |
Eosinophilia, Tropical |
Hemic and Lymphatic Diseases |
| C0014474 |
BXGD000917 |
Ependymoma |
Neoplasms |
| C0014518 |
BXGD000921 |
Toxic Epidermal Necrolysis |
Skin and Connective Tissue Diseases; Immune System Diseases; Chemically-Induced Disorders; Stomatognathic Diseases |
| C0014591 |
BXGD000938 |
Epistaxis |
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Otorhinolaryngologic Diseases |
| C0014772 |
BXGD000948 |
Red Blood Cell Count measurement |
|
| C0014800 |
BXGD000950 |
Erythroid hyperplasia |
Pathological Conditions, Signs and Symptoms |
| C0014804 |
BXGD000951 |
Erythromelalgia |
Cardiovascular Diseases |
| C0014859 |
BXGD000961 |
Esophageal Neoplasms |
Digestive System Diseases; Neoplasms |
| C0014867 |
BXGD000964 |
Esophageal Varices |
Digestive System Diseases |
| C0015302 |
BXGD000974 |
External exotoses |
Musculoskeletal Diseases |
| C0015625 |
BXGD001006 |
Fanconi Anemia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases |
| C0015672 |
BXGD001011 |
Fatigue |
Pathological Conditions, Signs and Symptoms |
| C0015695 |
BXGD001013 |
Fatty Liver |
Digestive System Diseases |
| C0015967 |
BXGD001030 |
Fever |
Pathological Conditions, Signs and Symptoms |
| C0016199 |
BXGD001049 |
Flank Pain |
Pathological Conditions, Signs and Symptoms |
| C0017181 |
BXGD001103 |
Gastrointestinal Hemorrhage |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C0017565 |
BXGD001118 |
Gingival Hemorrhage |
Pathological Conditions, Signs and Symptoms; Stomatognathic Diseases |
| C0017636 |
BXGD001131 |
Glioblastoma |
Neoplasms |
| C0017638 |
BXGD001132 |
Glioma |
Neoplasms |
| C0017925 |
BXGD001156 |
Glycogen Storage Disease Type VI |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0018133 |
BXGD001176 |
Graft-vs-Host Disease |
Immune System Diseases |
| C0018273 |
BXGD001189 |
Growth Disorders |
Pathological Conditions, Signs and Symptoms |
| C0018553 |
BXGD001203 |
Hamartoma Syndrome, Multiple |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms |
| C0018681 |
BXGD001214 |
Headache |
Pathological Conditions, Signs and Symptoms |
| C0018799 |
BXGD001224 |
Heart Diseases |
Cardiovascular Diseases |
| C0018801 |
BXGD001226 |
Heart failure |
Cardiovascular Diseases |
| C0018802 |
BXGD001227 |
Congestive heart failure |
Cardiovascular Diseases |
| C0018824 |
BXGD001237 |
Heart valve disease |
Cardiovascular Diseases |
| C0018916 |
BXGD001245 |
Hemangioma |
Neoplasms |
| C0018939 |
BXGD001253 |
Hematological Disease |
Hemic and Lymphatic Diseases |
| C0018952 |
BXGD001257 |
Extramedullary Hematopoiesis Function |
|
| C0019154 |
BXGD001291 |
Hepatic Vein Thrombosis |
Digestive System Diseases; Cardiovascular Diseases |
| C0019159 |
BXGD001294 |
Hepatitis A |
Digestive System Diseases; Infections |
| C0019207 |
BXGD001303 |
Hepatoma, Morris |
Digestive System Diseases; Neoplasms |
| C0019208 |
BXGD001304 |
Hepatoma, Novikoff |
Digestive System Diseases; Neoplasms |
| 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 |
| C0019348 |
BXGD001325 |
Herpes Simplex Infections |
Infections; Skin and Connective Tissue Diseases |
| C0019621 |
BXGD001340 |
Histiocytosis, Langerhans-Cell |
Respiratory Tract Diseases; Hemic and Lymphatic Diseases |
| C0019829 |
BXGD001350 |
Hodgkin Disease |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0020429 |
BXGD001378 |
Hyperalgesia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0020456 |
BXGD001392 |
Hyperglycemia |
Nutritional and Metabolic Diseases |
| C0020458 |
BXGD001393 |
Hyperhidrosis disorder |
Skin and Connective Tissue Diseases |
| C0020459 |
BXGD001394 |
Hyperinsulinism |
Nutritional and Metabolic Diseases |
| C0020473 |
BXGD001396 |
Hyperlipidemia |
Nutritional and Metabolic Diseases |
| C0020517 |
BXGD001415 |
Hypersensitivity |
Immune System Diseases |
| C0020538 |
BXGD001422 |
Hypertensive disease |
Cardiovascular Diseases |
| C0020541 |
BXGD001424 |
Portal Hypertension |
Digestive System Diseases |
| C0020545 |
BXGD001427 |
Hypertension, Renovascular |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Cardiovascular Diseases |
| C0021368 |
BXGD001502 |
Inflammation |
Pathological Conditions, Signs and Symptoms |
| C0021390 |
BXGD001503 |
Inflammatory Bowel Diseases |
Digestive System Diseases |
| C0021775 |
BXGD001512 |
Intermittent Claudication |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0021843 |
BXGD001520 |
Intestinal Obstruction |
Digestive System Diseases |
| C0022346 |
BXGD001537 |
Icterus |
Pathological Conditions, Signs and Symptoms |
| C0022660 |
BXGD001571 |
Kidney Failure, Acute |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0022679 |
BXGD001575 |
Cystic kidney |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0022680 |
BXGD001576 |
Polycystic Kidney Diseases |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0022735 |
BXGD001581 |
Klinefelter Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases |
| C0023281 |
BXGD001628 |
Leishmaniasis |
Infections; Skin and Connective Tissue Diseases |
| C0023418 |
BXGD001642 |
leukemia |
Neoplasms |
| C0023434 |
BXGD001643 |
Chronic Lymphocytic Leukemia |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0023440 |
BXGD001646 |
Acute Erythroblastic Leukemia |
Neoplasms; Hemic and Lymphatic Diseases |
| C0023448 |
BXGD001649 |
Lymphoid leukemia |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| 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 |
| C0023462 |
BXGD001654 |
Acute Megakaryocytic Leukemias |
Neoplasms |
| C0023465 |
BXGD001656 |
Acute monocytic leukemia |
Neoplasms |
| C0023467 |
BXGD001658 |
Leukemia, Myelocytic, Acute |
Neoplasms |
| C0023470 |
BXGD001659 |
Myeloid Leukemia |
Neoplasms |
| C0023473 |
BXGD001661 |
Myeloid Leukemia, Chronic |
Neoplasms; Hemic and Lymphatic Diseases |
| C0023480 |
BXGD001664 |
Leukemia, Myelomonocytic, Chronic |
Neoplasms; Hemic and Lymphatic Diseases |
| C0023481 |
BXGD001665 |
Chronic Neutrophilic Leukemia |
Hemic and Lymphatic Diseases |
| C0023492 |
BXGD001671 |
Leukemia, T-Cell |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0023508 |
BXGD001675 |
White Blood Cell Count procedure |
|
| C0023518 |
BXGD001677 |
Leukocytosis |
Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases |
| C0023530 |
BXGD001683 |
Leukopenia |
Hemic and Lymphatic Diseases |
| C0023646 |
BXGD001690 |
Lichen Planus |
Skin and Connective Tissue Diseases |
| C0023890 |
BXGD001713 |
Liver Cirrhosis |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C0023892 |
BXGD001715 |
Biliary cirrhosis |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C0023893 |
BXGD001716 |
Liver Cirrhosis, Experimental |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C0023895 |
BXGD001717 |
Liver diseases |
Digestive System Diseases |
| C0023903 |
BXGD001720 |
Liver neoplasms |
Digestive System Diseases; Neoplasms |
| C0023904 |
BXGD001721 |
Liver Neoplasms, Experimental |
Digestive System Diseases; Neoplasms |
| C0024121 |
BXGD001735 |
Lung Neoplasms |
Neoplasms; Respiratory Tract Diseases |
| C0024141 |
BXGD001740 |
Lupus Erythematosus, Systemic |
Skin and Connective Tissue Diseases; Immune System Diseases |
| C0024299 |
BXGD001758 |
Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0024305 |
BXGD001763 |
Lymphoma, Non-Hodgkin |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0024314 |
BXGD001767 |
Lymphoproliferative Disorders |
Immune System Diseases; Hemic and Lymphatic Diseases |
| C0024523 |
BXGD001781 |
Malabsorption Syndrome |
Digestive System Diseases; Nutritional and Metabolic Diseases |
| C0024623 |
BXGD001791 |
Malignant neoplasm of stomach |
Digestive System Diseases; Neoplasms |
| C0024790 |
BXGD001804 |
Paroxysmal nocturnal hemoglobinuria |
Hemic and Lymphatic Diseases |
| C0024894 |
BXGD001810 |
Mastitis |
Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases |
| C0024899 |
BXGD001812 |
Mastocytosis |
Neoplasms; Skin and Connective Tissue Diseases; Immune System Diseases |
| C0025149 |
BXGD001826 |
Medulloblastoma |
Neoplasms |
| C0025167 |
BXGD001829 |
Megakaryocytic hyperplasia |
Pathological Conditions, Signs and Symptoms |
| C0025202 |
BXGD001832 |
melanoma |
Neoplasms |
| C0025286 |
BXGD001850 |
Meningioma |
Neoplasms; Nervous System Diseases |
| C0025322 |
BXGD001863 |
Premature Menopause |
Female Urogenital Diseases and Pregnancy Complications |
| C0025472 |
BXGD001872 |
Mesenteric Vascular Occlusion |
Digestive System Diseases; Cardiovascular Diseases |
| C0026277 |
BXGD001899 |
Mixed Salivary Gland Tumor |
Neoplasms |
| C0026470 |
BXGD001903 |
Monoclonal Gammopathy of Undetermined Significance |
Immune System Diseases; Hemic and Lymphatic 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 |
| C0026948 |
BXGD001952 |
Mycosis Fungoides |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0026985 |
BXGD001956 |
Myelodysplasia |
|
| C0026987 |
BXGD001957 |
Myelofibrosis |
Pathological Conditions, Signs and Symptoms; Neoplasms; Hemic and Lymphatic Diseases |
| C0026998 |
BXGD001959 |
Acute Myeloid Leukemia, M1 |
Neoplasms |
| C0027013 |
BXGD001960 |
Myeloid Metaplasia |
Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases |
| C0027022 |
BXGD001962 |
Myeloproliferative disease |
Hemic and Lymphatic Diseases |
| C0027051 |
BXGD001963 |
Myocardial Infarction |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0027055 |
BXGD001964 |
Myocardial Reperfusion Injury |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0027059 |
BXGD001965 |
Myocarditis |
Cardiovascular Diseases |
| C0027627 |
BXGD002006 |
Neoplasm Metastasis |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0027651 |
BXGD002009 |
Neoplasms |
Neoplasms |
| C0027708 |
BXGD002025 |
Nephroblastoma |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0027796 |
BXGD002037 |
Neuralgia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0027819 |
BXGD002043 |
Neuroblastoma |
Neoplasms |
| C0027831 |
BXGD002047 |
Neurofibromatosis 1 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nervous System Diseases |
| C0027947 |
BXGD002061 |
Neutropenia |
Hemic and Lymphatic Diseases |
| C0028754 |
BXGD002082 |
Obesity |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases |
| C0029408 |
BXGD002137 |
Degenerative polyarthritis |
Musculoskeletal Diseases |
| C0029456 |
BXGD002157 |
Osteoporosis |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C0029463 |
BXGD002160 |
Osteosarcoma |
Neoplasms |
| C0029464 |
BXGD002161 |
Osteosclerosis |
Musculoskeletal Diseases |
| C0030193 |
BXGD002191 |
Pain |
Pathological Conditions, Signs and Symptoms |
| C0030232 |
BXGD002197 |
Pallor |
Pathological Conditions, Signs and Symptoms |
| C0030297 |
BXGD002204 |
Pancreatic Neoplasm |
Digestive System Diseases; Neoplasms; Endocrine System Diseases |
| C0030305 |
BXGD002206 |
Pancreatitis |
Digestive System Diseases |
| C0030312 |
BXGD002207 |
Pancytopenia |
Hemic and Lymphatic Diseases |
| C0030554 |
BXGD002239 |
Paresthesia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0031069 |
BXGD002279 |
Familial Mediterranean Fever |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C0031154 |
BXGD002291 |
Peritonitis |
Digestive System Diseases; Infections |
| C0031256 |
BXGD002296 |
Petechiae |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases; Cardiovascular Diseases |
| C0032109 |
BXGD002329 |
Plasma cell mastitis |
Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases |
| C0032181 |
BXGD002332 |
Platelet Count measurement |
|
| C0032460 |
BXGD002355 |
Polycystic Ovary Syndrome |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C0032461 |
BXGD002356 |
Polycythemia |
Hemic and Lymphatic Diseases |
| C0032463 |
BXGD002357 |
Polycythemia Vera |
Neoplasms; Hemic and Lymphatic Diseases |
| C0032962 |
BXGD002382 |
Pregnancy Complications |
Female Urogenital Diseases and Pregnancy Complications |
| C0033578 |
BXGD002408 |
Prostatic Neoplasms |
Neoplasms; Male Urogenital Diseases |
| C0033774 |
BXGD002419 |
Pruritus |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases |
| C0033860 |
BXGD002438 |
Psoriasis |
Skin and Connective Tissue Diseases |
| C0034065 |
BXGD002454 |
Pulmonary Embolism |
Respiratory Tract Diseases; Cardiovascular Diseases |
| C0034067 |
BXGD002456 |
Pulmonary Emphysema |
Respiratory Tract Diseases |
| C0034069 |
BXGD002458 |
Pulmonary Fibrosis |
Respiratory Tract Diseases |
| C0034150 |
BXGD002466 |
Purpura |
Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases |
| C0034155 |
BXGD002468 |
Purpura, Thrombotic Thrombocytopenic |
Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases |
| C0035067 |
BXGD002504 |
Renal Artery Stenosis |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Cardiovascular Diseases |
| C0035229 |
BXGD002516 |
Respiratory Insufficiency |
Respiratory Tract Diseases |
| C0035305 |
BXGD002529 |
Retinal Detachment |
Eye Diseases |
| C0035328 |
BXGD002537 |
Retinal Vein Occlusion |
Eye Diseases; Cardiovascular Diseases |
| C0036421 |
BXGD002613 |
Systemic Scleroderma |
Skin and Connective Tissue Diseases |
| C0036572 |
BXGD002625 |
Seizures |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0036690 |
BXGD002632 |
Septicemia |
Pathological Conditions, Signs and Symptoms; Infections |
| C0036920 |
BXGD002645 |
Sezary Syndrome |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0037274 |
BXGD002676 |
Dermatologic disorders |
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 |
| C0038013 |
BXGD002725 |
Ankylosing spondylitis |
Musculoskeletal Diseases |
| C0038454 |
BXGD002760 |
Cerebrovascular accident |
Nervous System Diseases; Cardiovascular Diseases |
| C0038525 |
BXGD002768 |
Subarachnoid Hemorrhage |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases |
| C0039070 |
BXGD002787 |
Syncope |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0039240 |
BXGD002804 |
Supraventricular tachycardia |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0039263 |
BXGD002805 |
Takayasu Arteritis |
Skin and Connective Tissue Diseases; Cardiovascular Diseases |
| C0039730 |
BXGD002826 |
Thalassemia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0039841 |
BXGD002829 |
Thiamine Deficiency |
Nutritional and Metabolic Diseases |
| C0040028 |
BXGD002835 |
Thrombocythemia, Essential |
Hemic and Lymphatic Diseases |
| C0040034 |
BXGD002836 |
Thrombocytopenia |
Hemic and Lymphatic Diseases |
| C0040038 |
BXGD002837 |
Thromboembolism |
Cardiovascular Diseases |
| C0040053 |
BXGD002839 |
Thrombosis |
Cardiovascular Diseases |
| C0040100 |
BXGD002840 |
Thymoma |
Neoplasms; Hemic and Lymphatic Diseases |
| C0040264 |
BXGD002857 |
Tinnitus |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases |
| C0040517 |
BXGD002872 |
Gilles de la Tourette syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders |
| C0040997 |
BXGD002894 |
Trigeminal Neuralgia |
Nervous System Diseases; Stomatognathic Diseases |
| C0041296 |
BXGD002903 |
Tuberculosis |
Infections |
| C0041956 |
BXGD002942 |
Ureteral obstruction |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0042170 |
BXGD002969 |
Uveomeningoencephalitic Syndrome |
Eye Diseases; Immune System Diseases; Nervous System Diseases |
| C0042487 |
BXGD002986 |
Venous Thrombosis |
Cardiovascular Diseases |
| C0042571 |
BXGD002991 |
Vertigo |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases |
| C0043121 |
BXGD003030 |
Wernicke Encephalopathy |
Nutritional and Metabolic Diseases; Nervous System Diseases; Chemically-Induced Disorders; Mental Disorders |
| C0079731 |
BXGD003087 |
B-Cell Lymphomas |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0079744 |
BXGD003090 |
Diffuse Large B-Cell Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0079748 |
BXGD003094 |
Precursor cell lymphoblastic lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0079772 |
BXGD003099 |
T-Cell Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0079773 |
BXGD003100 |
Lymphoma, T-Cell, Cutaneous |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0085096 |
BXGD003123 |
Peripheral Vascular Diseases |
Cardiovascular Diseases |
| C0085110 |
BXGD003126 |
Severe Combined Immunodeficiency |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases |
| C0085215 |
BXGD003141 |
Ovarian Failure, Premature |
Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C0085413 |
BXGD003171 |
Polycystic Kidney, Autosomal Dominant |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0085642 |
BXGD003220 |
Livedo Reticularis |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases; Cardiovascular Diseases |
| C0085652 |
BXGD003224 |
Pyoderma Gangrenosum |
Skin and Connective Tissue Diseases |
| C0085669 |
BXGD003233 |
Acute leukemia |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0085702 |
BXGD003247 |
Monocytosis |
Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases |
| C0086404 |
BXGD003278 |
Experimental Hepatoma |
Digestive System Diseases; Neoplasms |
| C0149793 |
BXGD003366 |
Amaurosis Fugax |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C0149871 |
BXGD003375 |
Deep Vein Thrombosis |
Cardiovascular Diseases |
| C0149925 |
BXGD003387 |
Small cell carcinoma of lung |
Neoplasms; Respiratory Tract Diseases |
| C0151529 |
BXGD003433 |
Prolonged bleeding time |
|
| C0151744 |
BXGD003469 |
Myocardial Ischemia |
Cardiovascular Diseases |
| C0151825 |
BXGD003481 |
Bone pain |
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases |
| C0151942 |
BXGD003507 |
Arterial thrombosis |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0151945 |
BXGD003508 |
Thrombosis of cerebral veins |
Nervous System Diseases; Cardiovascular Diseases |
| C0152013 |
BXGD003516 |
Adenocarcinoma of lung (disorder) |
Neoplasms |
| C0152018 |
BXGD003518 |
Esophageal carcinoma |
Digestive System Diseases; Neoplasms |
| C0152264 |
BXGD003577 |
Familial erythrocytosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0152268 |
BXGD003580 |
Nodular Sclerosis Classical Hodgkin Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0152276 |
BXGD003581 |
Granulocytic Sarcoma |
Neoplasms |
| C0153426 |
BXGD003642 |
Malignant neoplasm of duodenum |
Digestive System Diseases; Neoplasms |
| C0153452 |
BXGD003647 |
Malignant neoplasm of gallbladder |
Digestive System Diseases; Neoplasms |
| C0153676 |
BXGD003679 |
Secondary malignant neoplasm of lung |
Neoplasms; Respiratory Tract Diseases |
| C0155626 |
BXGD003806 |
Acute myocardial infarction |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0155773 |
BXGD003820 |
Portal Vein Thrombosis |
Cardiovascular Diseases |
| C0160390 |
BXGD003921 |
Injury of liver |
Digestive System Diseases; Wounds and Injuries |
| C0162557 |
BXGD003956 |
Liver Failure, Acute |
Digestive System Diseases |
| C0175703 |
BXGD004009 |
Thrombocytopenia-Absent Radius Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Hemic and Lymphatic Diseases |
| C0178874 |
BXGD004037 |
Tumor Progression |
Pathological Conditions, Signs and Symptoms |
| C0200638 |
BXGD004043 |
Eosinophil count procedure |
|
| C0200641 |
BXGD004044 |
Blood basophil count (lab test) |
|
| C0202117 |
BXGD004074 |
Low density lipoprotein cholesterol measurement |
|
| C0206138 |
BXGD004158 |
CREST Syndrome |
Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Cardiovascular Diseases |
| C0206141 |
BXGD004160 |
Idiopathic Hypereosinophilic Syndrome |
Hemic and Lymphatic Diseases |
| C0220597 |
BXGD004292 |
Adult Hodgkin Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0220621 |
BXGD004300 |
Childhood Acute Myeloid Leukemia |
Neoplasms |
| C0220630 |
BXGD004302 |
Adult Liver Carcinoma |
Digestive System Diseases; Neoplasms |
| C0220644 |
BXGD004306 |
Childhood Hodgkin Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0220650 |
BXGD004310 |
Metastatic malignant neoplasm to brain |
Pathological Conditions, Signs and Symptoms; Neoplasms; Nervous System Diseases |
| C0220756 |
BXGD004338 |
Niemann-Pick Disease, Type C |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Hemic and Lymphatic Diseases |
| C0221002 |
BXGD004360 |
Hyperparathyroidism, Primary |
Endocrine System Diseases |
| C0221013 |
BXGD004363 |
Mastocytosis, Systemic |
Neoplasms; Immune System Diseases |
| C0221281 |
BXGD004436 |
Poikilocytosis |
|
| C0231807 |
BXGD004524 |
Dyspnea on exertion |
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases |
| C0232370 |
BXGD004541 |
Florid red complexion (finding) |
|
| C0235031 |
BXGD004714 |
Neurologic Symptoms |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0235782 |
BXGD004769 |
Gallbladder Carcinoma |
Digestive System Diseases; Neoplasms |
| C0235974 |
BXGD004796 |
Pancreatic carcinoma |
Digestive System Diseases; Neoplasms; Endocrine System Diseases |
| C0238461 |
BXGD004936 |
Anaplastic thyroid carcinoma |
Neoplasms |
| C0238694 |
BXGD004953 |
Peripheral arthritis |
Musculoskeletal Diseases |
| C0239574 |
BXGD004986 |
Low grade fever |
Pathological Conditions, Signs and Symptoms |
| C0239935 |
BXGD005007 |
Hematocrit increased |
|
| C0239946 |
BXGD005010 |
Fibrosis, Liver |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C0240912 |
BXGD005062 |
Vertical Talus |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0241144 |
BXGD005080 |
Petechiae of skin |
Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases |
| C0241868 |
BXGD005118 |
acute aortic dissection |
Cardiovascular Diseases |
| C0242006 |
BXGD005132 |
Myelofibrosis due to another disorder |
|
| C0242339 |
BXGD005150 |
Dyslipidemias |
Nutritional and Metabolic Diseases |
| C0242379 |
BXGD005157 |
Malignant neoplasm of lung |
Neoplasms; Respiratory Tract Diseases |
| C0242584 |
BXGD005179 |
Autoimmune thrombocytopenia |
Immune System Diseases; Hemic and Lymphatic Diseases |
| C0242596 |
BXGD005181 |
Neoplasm, Residual |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0242621 |
BXGD005183 |
Isochromosomes |
Pathological Conditions, Signs and Symptoms |
| C0242647 |
BXGD005184 |
Mucosa-Associated Lymphoid Tissue Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0243026 |
BXGD005210 |
Sepsis |
Pathological Conditions, Signs and Symptoms; Infections |
| C0263628 |
BXGD005334 |
Tumoral calcinosis |
Nutritional and Metabolic Diseases |
| C0263662 |
BXGD005339 |
Disseminated eosinophilic collagen disease |
Skin and Connective Tissue Diseases |
| C0265219 |
BXGD005468 |
Miller Dieker syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0267953 |
BXGD005795 |
Necrosis of pancreas |
Digestive System Diseases |
| C0271561 |
BXGD006213 |
Somatotropin deficiency |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Endocrine System Diseases |
| C0271979 |
BXGD006283 |
Thalassemia Intermedia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0272286 |
BXGD006337 |
Thrombocytopenia due to platelet alloimmunization |
Hemic and Lymphatic Diseases |
| C0272362 |
BXGD006357 |
Acquired von Willebrand's disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0278510 |
BXGD006526 |
Childhood Medulloblastoma |
Neoplasms |
| C0278721 |
BXGD006572 |
Adult Lymphoblastic Lymphoma |
|
| C0278764 |
BXGD006581 |
Adult Burkitt Lymphoma |
Neoplasms; Infections; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0278876 |
BXGD006607 |
Adult Medulloblastoma |
Neoplasms |
| C0278878 |
BXGD006609 |
Adult Glioblastoma |
Neoplasms |
| C0278879 |
BXGD006610 |
Childhood Burkitt Lymphoma |
Neoplasms; Infections; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0279000 |
BXGD006622 |
Liver and Intrahepatic Biliary Tract Carcinoma |
Digestive System Diseases; Neoplasms |
| C0279525 |
BXGD006627 |
Childhood Lymphoblastic Lymphoma |
|
| C0279530 |
BXGD006628 |
Malignant Bone Neoplasm |
Neoplasms; Musculoskeletal Diseases |
| C0279543 |
BXGD006630 |
Philadelphia chromosome positive chronic myelogenous leukemia |
Neoplasms; Hemic and Lymphatic Diseases |
| C0279549 |
BXGD006634 |
Philadelphia chromosome negative chronic myelogenous leukemia |
Neoplasms; Hemic and Lymphatic Diseases |
| C0279583 |
BXGD006640 |
Childhood T Acute Lymphoblastic Leukemia |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0279584 |
BXGD006641 |
Childhood B Acute Lymphoblastic Leukemia |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0279593 |
BXGD006644 |
Adult B Acute Lymphoblastic Leukemia |
|
| C0279626 |
BXGD006657 |
Squamous cell carcinoma of esophagus |
Digestive System Diseases; Neoplasms |
| C0279628 |
BXGD006659 |
Adenocarcinoma Of Esophagus |
Digestive System Diseases; Neoplasms |
| C0279629 |
BXGD006660 |
Adult Acute Monoblastic Leukemia |
Neoplasms |
| C0279645 |
BXGD006669 |
Childhood Acute Monoblastic Leukemia |
|
| C0279651 |
BXGD006674 |
Gallbladder adenocarcinoma |
Digestive System Diseases; Neoplasms |
| C0279702 |
BXGD006685 |
Conventional (Clear Cell) Renal Cell Carcinoma |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0279751 |
BXGD006694 |
Adenoid cystic carcinoma of salivary gland |
Neoplasms; Stomatognathic Diseases |
| C0280100 |
BXGD006713 |
Solid Neoplasm |
Neoplasms |
| C0280449 |
BXGD006746 |
secondary acute myeloid leukemia |
Neoplasms |
| C0280451 |
BXGD006747 |
de novo myelodysplastic syndromes |
Hemic and Lymphatic Diseases |
| C0280474 |
BXGD006748 |
Childhood Glioblastoma |
Neoplasms |
| C0302486 |
BXGD006847 |
Erythrophagocytosis |
|
| C0302592 |
BXGD006851 |
Cervix carcinoma |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications |
| C0333307 |
BXGD006946 |
Superficial ulcer |
Pathological Conditions, Signs and Symptoms |
| C0334674 |
BXGD007151 |
Acute panmyelosis with myelofibrosis |
Neoplasms; Hemic and Lymphatic Diseases |
| C0338573 |
BXGD007199 |
Cerebral venous sinus thrombosis |
Nervous System Diseases; Cardiovascular Diseases |
| C0338575 |
BXGD007200 |
Sagittal Sinus Thrombosis |
Nervous System Diseases; Cardiovascular Diseases |
| C0338656 |
BXGD007211 |
Impaired cognition |
Mental Disorders |
| C0341439 |
BXGD007408 |
Chronic liver disease |
Digestive System Diseases |
| C0344315 |
BXGD007666 |
Depressed mood |
Behavior and Behavior Mechanisms |
| C0345904 |
BXGD007745 |
Malignant neoplasm of liver |
Digestive System Diseases; Neoplasms |
| C0346153 |
BXGD007781 |
Breast Cancer, Familial |
Neoplasms; Skin and Connective Tissue Diseases |
| C0346302 |
BXGD007807 |
Growth Hormone-Secreting Pituitary Adenoma |
Neoplasms; Nervous System Diseases; Endocrine System Diseases |
| C0346421 |
BXGD007827 |
Chronic eosinophilic leukemia |
Neoplasms; Hemic and Lymphatic Diseases |
| C0346647 |
BXGD007832 |
Malignant neoplasm of pancreas |
Digestive System Diseases; Neoplasms; Endocrine System Diseases |
| C0346976 |
BXGD007838 |
Secondary malignant neoplasm of pancreas |
Digestive System Diseases; Neoplasms; Endocrine System Diseases |
| C0349464 |
BXGD007908 |
Wernicke-Korsakoff Syndrome |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms |
| C0349532 |
BXGD007917 |
Gastric lymphoma |
Digestive System Diseases; Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0349636 |
BXGD007941 |
Pre B-cell acute lymphoblastic leukemia |
|
| C0349639 |
BXGD007943 |
Juvenile Myelomonocytic Leukemia |
Neoplasms; Hemic and Lymphatic Diseases |
| 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 |
| C0376544 |
BXGD008001 |
Hematopoietic Neoplasms |
Neoplasms; Hemic and Lymphatic Diseases |
| C0376545 |
BXGD008002 |
Hematologic Neoplasms |
Neoplasms; Hemic and Lymphatic Diseases |
| C0392885 |
BXGD008071 |
High density lipoprotein measurement |
|
| C0393642 |
BXGD008111 |
Sepsis-Associated Encephalopathy |
Nervous System Diseases |
| C0393706 |
BXGD008126 |
Early infantile epileptic encephalopathy with suppression bursts |
Nervous System Diseases |
| C0398623 |
BXGD008202 |
Thrombophilia |
Hemic and Lymphatic Diseases |
| C0398650 |
BXGD008212 |
Immune thrombocytopenic purpura |
Pathological Conditions, Signs and Symptoms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0400966 |
BXGD008266 |
Non-alcoholic Fatty Liver Disease |
Digestive System Diseases |
| C0410000 |
BXGD008406 |
Overlap syndrome |
Skin and Connective Tissue Diseases; Immune System Diseases |
| C0423798 |
BXGD008510 |
Increased tendency to bruise |
Wounds and Injuries |
| C0424295 |
BXGD008524 |
Hyperactive behavior |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0432411 |
BXGD008787 |
Chromosome 9, trisomy |
Pathological Conditions, Signs and Symptoms |
| C0432474 |
BXGD008793 |
Klinefelter's syndrome - male with more than two X chromosomes |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases |
| C0456863 |
BXGD008879 |
High grade B-cell lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0457334 |
BXGD008888 |
Acute monoblastic leukemia |
Neoplasms |
| C0457506 |
BXGD008889 |
Reactive thrombocytosis |
Hemic and Lymphatic Diseases |
| C0497156 |
BXGD009053 |
Lymphadenopathy |
Hemic and Lymphatic Diseases |
| C0521158 |
BXGD009130 |
Recurrent tumor |
|
| C0521174 |
BXGD009133 |
Microcalcification |
Nutritional and Metabolic Diseases |
| C0521607 |
BXGD009146 |
Peritoneal Fibrosis |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C0524528 |
BXGD009229 |
Pervasive Development Disorder |
Mental Disorders |
| C0524620 |
BXGD009236 |
Metabolic Syndrome X |
Nutritional and Metabolic Diseases |
| C0541912 |
BXGD009264 |
Duodenal Cancer |
Digestive System Diseases; Neoplasms |
| C0544886 |
BXGD009319 |
Somatic mutation |
|
| C0546837 |
BXGD009343 |
Malignant neoplasm of esophagus |
Digestive System Diseases; Neoplasms |
| C0549448 |
BXGD009381 |
Hemoglobin increased |
Neoplasms; Hemic and Lymphatic Diseases |
| C0578575 |
BXGD009550 |
Dissection of proximal aorta |
|
| C0584960 |
BXGD009579 |
Factor V Leiden mutation |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0585442 |
BXGD009593 |
Osteosarcoma of bone |
Neoplasms |
| C0588125 |
BXGD009621 |
Nodular tenosynovitis |
Neoplasms; Musculoskeletal Diseases |
| C0596263 |
BXGD009639 |
Carcinogenesis |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0598608 |
BXGD009668 |
Hyperhomocysteinemia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0598766 |
BXGD009669 |
Leukemogenesis |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0598798 |
BXGD009672 |
Lymphoid neoplasm |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0598935 |
BXGD009674 |
Tumor Initiation |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0600139 |
BXGD009695 |
Prostate carcinoma |
Neoplasms; Male Urogenital Diseases |
| C0600433 |
BXGD009707 |
Activated Protein C Resistance |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0600502 |
BXGD009710 |
Vascular Hemostatic Disorders |
Hemic and Lymphatic Diseases; Cardiovascular Diseases |
| C0677060 |
BXGD009716 |
essential thrombocytopenia |
Pathological Conditions, Signs and Symptoms; Immune System Diseases; Hemic and Lymphatic 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 |
| C0684249 |
BXGD009790 |
Carcinoma of lung |
Neoplasms; Respiratory Tract Diseases |
| C0686619 |
BXGD009835 |
Secondary malignant neoplasm of lymph node |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0699790 |
BXGD009866 |
Colon Carcinoma |
Digestive System Diseases; Neoplasms |
| C0699791 |
BXGD009867 |
Stomach Carcinoma |
Digestive System Diseases; Neoplasms |
| C0699885 |
BXGD009869 |
Carcinoma of bladder |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0700095 |
BXGD009875 |
Central neuroblastoma |
Neoplasms; Nervous System Diseases |
| C0740302 |
BXGD009975 |
5q-syndrome |
Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases |
| C0740391 |
BXGD009987 |
Middle Cerebral Artery Occlusion |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases |
| C0740394 |
BXGD009989 |
Hyperuricemia |
Pathological Conditions, Signs and Symptoms |
| C0740992 |
BXGD010020 |
anemia hemoglobin |
|
| C0742343 |
BXGD010061 |
Acute Chest Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Hemic and Lymphatic Diseases |
| C0745091 |
BXGD010113 |
Hypereosinophilia |
Hemic and Lymphatic Diseases |
| C0745744 |
BXGD010133 |
End Stage Liver Disease |
Digestive System Diseases |
| C0751074 |
BXGD010313 |
Diabetic Neuralgia |
Nervous System Diseases; Endocrine System Diseases |
| C0751606 |
BXGD010523 |
Adult Acute Lymphocytic Leukemia |
|
| C0752355 |
BXGD010725 |
Myotonia Fluctuans (disorder) |
Musculoskeletal Diseases; Nervous System Diseases |
| C0836924 |
BXGD010864 |
Thrombocytosis |
Hemic and Lymphatic Diseases |
| C0852949 |
BXGD010957 |
Arteriopathic disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0855082 |
BXGD011069 |
Refractory Hodgkin Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0855742 |
BXGD011087 |
Abnormal platelet morphology |
|
| C0856761 |
BXGD011115 |
Budd-Chiari Syndrome |
Digestive System Diseases; Cardiovascular Diseases |
| C0856825 |
BXGD011118 |
Acute GVH disease |
Immune System Diseases |
| C0860207 |
BXGD011220 |
Drug-Induced Liver Disease |
Digestive System Diseases; Chemically-Induced Disorders |
| C0917798 |
BXGD011409 |
Cerebral Ischemia |
Nervous System Diseases; Cardiovascular Diseases |
| C0917805 |
BXGD011414 |
Transient Cerebral Ischemia |
Nervous System Diseases; Cardiovascular Diseases |
| C0919267 |
BXGD011426 |
ovarian neoplasm |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C0919747 |
BXGD011439 |
Cytokine storm |
|
| C0948008 |
BXGD011499 |
Ischemic stroke |
Nervous System Diseases; Cardiovascular Diseases |
| C0948089 |
BXGD011504 |
Acute Coronary Syndrome |
Cardiovascular Diseases |
| C1140680 |
BXGD011718 |
Malignant neoplasm of ovary |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C1167791 |
BXGD011776 |
Skin toxicity |
|
| C1168401 |
BXGD011792 |
Squamous cell carcinoma of the head and neck |
Neoplasms |
| C1261473 |
BXGD011855 |
Sarcoma |
Neoplasms |
| C1261502 |
BXGD011856 |
Finding of Mean Corpuscular Hemoglobin |
|
| C1262313 |
BXGD011881 |
Invasive Fungal Infections |
Infections |
| C1262477 |
BXGD011882 |
Weight decreased |
Pathological Conditions, Signs and Symptoms |
| C1264195 |
BXGD011913 |
Refractory anemia with ringed sideroblasts |
Hemic and Lymphatic Diseases |
| C1268935 |
BXGD011997 |
Congenital Thrombotic Thrombocytopenic Purpura |
Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases |
| C1268964 |
BXGD012000 |
Myelodysplastic syndrome, no ICD-O subtype |
Hemic and Lymphatic Diseases |
| C1269955 |
BXGD012005 |
Tumor Cell Invasion |
|
| C1275685 |
BXGD012092 |
Avellino corneal dystrophy |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C1276092 |
BXGD012105 |
Chronic hand eczema |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases |
| C1279296 |
BXGD012118 |
Chronic leukemia (category) |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C1282609 |
BXGD012149 |
Granulocytosis |
Hemic and Lymphatic Diseases |
| C1292754 |
BXGD012227 |
Mediastinal (Thymic) Large B-Cell Lymphoma |
Neoplasms; Respiratory Tract Diseases; Immune System Diseases; Hemic and Lymphatic Diseases |
| C1292758 |
BXGD012229 |
Precursor T-cell lymphoblastic lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C1292769 |
BXGD012230 |
Precursor B-cell lymphoblastic leukemia |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C1292772 |
BXGD012232 |
Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative |
Neoplasms; Hemic and Lymphatic Diseases |
| C1292778 |
BXGD012237 |
Chronic myeloproliferative disorder |
Neoplasms; Hemic and Lymphatic Diseases |
| C1292779 |
BXGD012238 |
Myelodysplastic Syndrome with Isolated del(5q) |
Hemic and Lymphatic Diseases |
| C1301355 |
BXGD012287 |
Myelodysplastic-Myeloproliferative Diseases |
Hemic and Lymphatic Diseases |
| C1306459 |
BXGD012361 |
Primary malignant neoplasm |
Neoplasms |
| C1306460 |
BXGD012362 |
Primary malignant neoplasm of lung |
Neoplasms; Respiratory Tract Diseases |
| C1306759 |
BXGD012374 |
Eosinophilic disorder |
Hemic and Lymphatic Diseases |
| C1318533 |
BXGD012398 |
Secondary polycythemia |
Neoplasms; Hemic and Lymphatic Diseases |
| C1318543 |
BXGD012400 |
Fibrous histiocytoma of tendon sheath |
Neoplasms; Musculoskeletal Diseases |
| C1328061 |
BXGD012459 |
Myelodysplastic/myeloproliferative neoplasm, unclassifiable |
Hemic and Lymphatic Diseases |
| C1328504 |
BXGD012469 |
Hormone refractory prostate cancer |
Neoplasms; Male Urogenital Diseases |
| C1332201 |
BXGD012502 |
Adult Diffuse Large B-Cell Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C1332206 |
BXGD012504 |
Adult Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C1332213 |
BXGD012507 |
Adult T Lymphoblastic Lymphoma |
|
| C1332970 |
BXGD012568 |
Childhood Hematopoietic Neoplasm |
Neoplasms; Hemic and Lymphatic Diseases |
| C1332977 |
BXGD012569 |
Childhood Leukemia |
Neoplasms |
| C1332979 |
BXGD012571 |
Childhood Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C1332986 |
BXGD012574 |
Childhood Osteosarcoma |
Neoplasms |
| C1332998 |
BXGD012577 |
Childhood T Lymphoblastic Lymphoma |
|
| C1333046 |
BXGD012585 |
Myeloproliferative Neoplasm, Unclassifiable |
|
| C1333064 |
BXGD012587 |
Classical Hodgkin's Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C1334665 |
BXGD012726 |
Mediastinal Lymphoma |
Neoplasms; Respiratory Tract Diseases |
| C1334968 |
BXGD012749 |
Nodular Lymphocyte Predominant Hodgkin Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C1335177 |
BXGD012771 |
Ovarian Serous Adenocarcinoma |
Neoplasms |
| C1367654 |
BXGD012886 |
Marginal Zone B-Cell Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C1378511 |
BXGD012932 |
Undifferentiated leukemia |
|
| C1391732 |
BXGD012971 |
Cancer cachexia |
|
| C1445957 |
BXGD013081 |
Serum total cholesterol measurement |
|
| C1458140 |
BXGD013134 |
Bleeding tendency |
Hemic and Lymphatic Diseases |
| C1458155 |
BXGD013136 |
Mammary Neoplasms |
Neoplasms; Skin and Connective Tissue Diseases |
| C1510586 |
BXGD013176 |
Autism Spectrum Disorders |
Mental Disorders |
| C1512409 |
BXGD013188 |
Hepatocarcinogenesis |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C1512694 |
BXGD013193 |
Increased Cellularity Present |
|
| C1512981 |
BXGD013196 |
Mammary Tumorigenesis |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C1516553 |
BXGD013216 |
Prefibrotic/Early Primary Myelofibrosis |
Hemic and Lymphatic Diseases |
| C1519670 |
BXGD013241 |
Tumor Angiogenesis |
Pathological Conditions, Signs and Symptoms |
| C1521897 |
BXGD013251 |
Mature T ALL |
|
| C1527304 |
BXGD013266 |
Allergic Reaction |
Immune System Diseases |
| C1527405 |
BXGD013290 |
Erythrocytosis |
Hemic and Lymphatic Diseases |
| C1531624 |
BXGD013300 |
Cardioembolic stroke |
|
| C1540912 |
BXGD013349 |
Hypereosinophilic syndrome |
Hemic and Lymphatic Diseases |
| C1561643 |
BXGD013363 |
Chronic Kidney Diseases |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C1608408 |
BXGD013434 |
Malignant transformation |
|
| C1611743 |
BXGD013456 |
Familial (FPAH) |
|
| C1621958 |
BXGD013468 |
Glioblastoma Multiforme |
Neoplasms |
| C1623038 |
BXGD013475 |
Cirrhosis |
Pathological Conditions, Signs and Symptoms |
| C1658953 |
BXGD013486 |
tumor vasculature |
|
| C1704272 |
BXGD013537 |
Benign Prostatic Hyperplasia |
Male Urogenital Diseases |
| C1704436 |
BXGD013564 |
Peripheral Arterial Diseases |
Cardiovascular Diseases |
| C1708781 |
BXGD013613 |
Sarcomatoid carcinoma of the lung |
Neoplasms; Respiratory Tract Diseases |
| C1709527 |
BXGD013626 |
B Acute Lymphoblastic Leukemia with t(9;22)(q34.1;q11.2); BCR-ABL1 |
|
| C1800706 |
BXGD013755 |
Idiopathic Pulmonary Fibrosis |
Respiratory Tract Diseases |
| C1802398 |
BXGD013758 |
Chromosome 5, trisomy 5q |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C1832661 |
BXGD013866 |
ANOPHTHALMIA AND PULMONARY HYPOPLASIA |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Respiratory Tract Diseases |
| C1837098 |
BXGD014198 |
Easy fatigability |
|
| C1840264 |
BXGD014439 |
IMMUNE SUPPRESSION |
|
| C1845118 |
BXGD014713 |
SHORT STATURE, IDIOPATHIC, X-LINKED |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C1848701 |
BXGD014967 |
Elevated hepatic transaminase |
|
| C1849749 |
BXGD015083 |
Peripheral thrombosis |
|
| C1852502 |
BXGD015286 |
CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT |
Musculoskeletal Diseases; Stomatognathic Diseases |
| C1853237 |
BXGD015319 |
Isolated cases |
|
| C1853288 |
BXGD015329 |
Increased red blood cell mass |
Hemic and Lymphatic Diseases |
| C1855472 |
BXGD015499 |
Acute lymphoblastic leukemia with lymphomatous features |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C1860320 |
BXGD015977 |
Bone marrow hypercellularity |
|
| C1861172 |
BXGD016016 |
Venous Thromboembolism |
Cardiovascular Diseases |
| C1861922 |
BXGD016094 |
CAMPOMELIC DYSPLASIA |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C1868683 |
BXGD016526 |
B-CELL MALIGNANCY, LOW-GRADE |
|
| C1879321 |
BXGD016572 |
Acute Myeloid Leukemia (AML-M2) |
Neoplasms |
| C1956089 |
BXGD016615 |
Osteophyte |
Musculoskeletal Diseases |
| C1956346 |
BXGD016627 |
Coronary Artery Disease |
Cardiovascular Diseases |
| C1961099 |
BXGD016672 |
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C1961102 |
BXGD016673 |
Precursor Cell Lymphoblastic Leukemia Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C1963099 |
BXGD016682 |
Myelodysplasia, CTCAE |
|
| C1963165 |
BXGD016685 |
Malabsorption, CTCAE |
|
| C2004493 |
BXGD016875 |
Leukemia, B-Cell |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C2239176 |
BXGD016965 |
Liver carcinoma |
Digestive System Diseases; Neoplasms |
| C2347507 |
BXGD017038 |
Childhood B Acute Lymphoblastic Leukemia with t(9;22)(q34.1;q11.2); BCR-ABL1 |
|
| C2347747 |
BXGD017040 |
Adult Classical Hodgkin Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C2347748 |
BXGD017041 |
Adult Erythroleukemia |
|
| C2347761 |
BXGD017049 |
Childhood Myelodysplastic Syndrome |
Hemic and Lymphatic Diseases |
| C2584620 |
BXGD017129 |
Thrombophilia, hereditary |
Hemic and Lymphatic Diseases |
| C2613439 |
BXGD017184 |
Extramedullary Hematopoiesis (disorder) |
Hemic and Lymphatic Diseases |
| C2675105 |
BXGD017271 |
BUDD-CHIARI SYNDROME, SUSCEPTIBILITY TO, SOMATIC |
|
| C2698259 |
BXGD017449 |
Monoclonal B-Cell Lymphocytosis |
Neoplasms; Hemic and Lymphatic Diseases |
| C2711227 |
BXGD017478 |
Steatohepatitis |
Digestive System Diseases |
| C2750440 |
BXGD017660 |
FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 1 |
|
| C2750441 |
BXGD017661 |
LIVER DISEASE, ALCOHOLIC, SUSCEPTIBILITY TO, 1 |
|
| C2826330 |
BXGD017791 |
Refractory anemia with ring sideroblasts associated with marked thrombocytosis |
Hemic and Lymphatic Diseases |
| C2827356 |
BXGD017793 |
Myeloid/Lymphoid Neoplasms with Eosinophilia and Rearrangement of PDGFRA, PDGFRB, or FGFR1, or with PCM1-JAK2 |
Neoplasms; Hemic and Lymphatic Diseases |
| C2827469 |
BXGD017798 |
Coronary Microvascular Disease |
|
| C2930974 |
BXGD017923 |
Acute erythroleukemia |
Neoplasms; Hemic and Lymphatic Diseases |
| C2931822 |
BXGD018068 |
Nasopharyngeal carcinoma |
Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases |
| C2936719 |
BXGD018130 |
Mechanical Allodynia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C2936904 |
BXGD018150 |
Opitz GBBB Syndrome, X-Linked |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases; Male Urogenital Diseases; Stomatognathic Diseases |
| C2937358 |
BXGD018159 |
Cerebral Hemorrhage |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases |
| C2939461 |
BXGD018180 |
Myeloid neoplasm |
Neoplasms; Hemic and Lymphatic Diseases |
| C2973725 |
BXGD018205 |
Pulmonary arterial hypertension |
Respiratory Tract Diseases; Cardiovascular Diseases |
| C2981142 |
BXGD018210 |
Refractory anemia, without ringed sideroblasts, without excess blasts |
Hemic and Lymphatic Diseases |
| C3150651 |
BXGD018316 |
FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 2 |
|
| C3150773 |
BXGD018336 |
CHROMOSOME 8p11 MYELOPROLIFERATIVE SYNDROME |
|
| C3152231 |
BXGD018463 |
Gastrointestinal infarctions |
|
| C3203102 |
BXGD018555 |
Idiopathic pulmonary arterial hypertension |
Respiratory Tract Diseases |
| C3241937 |
BXGD018578 |
Nonalcoholic Steatohepatitis |
Digestive System Diseases |
| C3266262 |
BXGD018600 |
Multiple Chronic Conditions |
Pathological Conditions, Signs and Symptoms |
| C3281125 |
BXGD018883 |
THROMBOCYTHEMIA 3 |
|
| C3463824 |
BXGD018899 |
MYELODYSPLASTIC SYNDROME |
Hemic and Lymphatic Diseases |
| C3469521 |
BXGD018910 |
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder) |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases |
| C3489628 |
BXGD018938 |
Thrombocytosis, Autosomal Dominant |
Hemic and Lymphatic Diseases |
| C3495676 |
BXGD019000 |
Anorectal Malformations |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases |
| C3539878 |
BXGD019087 |
Triple Negative Breast Neoplasms |
Neoplasms; Skin and Connective Tissue Diseases |
| C3665444 |
BXGD019288 |
Neutrophilia (disorder) |
Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases |
| C3714745 |
BXGD019427 |
Malabsorption |
Digestive System Diseases |
| C3714796 |
BXGD019434 |
Isolated somatotropin deficiency |
|
| C3805232 |
BXGD019469 |
Post polycythaemia vera myelofibrosis |
Neoplasms; Hemic and Lymphatic Diseases |
| C3830362 |
BXGD019751 |
Early Pregnancy Loss |
Female Urogenital Diseases and Pregnancy Complications |
| C3839741 |
BXGD019782 |
Core binding factor acute myeloid leukemia |
Neoplasms |
| C3839868 |
BXGD019788 |
Cytogenetically normal acute myeloid leukemia |
Neoplasms |
| C3875321 |
BXGD019874 |
Inflammatory dermatosis |
Skin and Connective Tissue Diseases |
| C3887524 |
BXGD019892 |
Skin Erosion |
Skin and Connective Tissue Diseases |
| C3887551 |
BXGD019898 |
Memory dysfunction |
Mental Disorders |
| C3887875 |
BXGD019923 |
Visual field defects |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C3888788 |
BXGD019984 |
Minimal hepatic encephalopathy |
|
| C3897729 |
BXGD020049 |
Refractory Childhood Hodgkin Lymphoma |
|
| C3899655 |
BXGD020091 |
Childhood Langerhans Cell Histiocytosis |
Respiratory Tract Diseases; Hemic and Lymphatic Diseases |
| C3900098 |
BXGD020106 |
Adult Myelodysplastic Syndrome |
Hemic and Lymphatic Diseases |
| C3900100 |
BXGD020108 |
Adult Langerhans Cell Histiocytosis |
Respiratory Tract Diseases; Hemic and Lymphatic Diseases |
| C4016234 |
BXGD020292 |
ERYTHROCYTOSIS, JAK2-RELATED, SOMATIC |
|
| C4022560 |
BXGD020916 |
Splanchnic vein thrombosis |
Cardiovascular Diseases |
| C4023026 |
BXGD021072 |
Abnormal megakaryocyte morphology |
|
| C4025187 |
BXGD021582 |
Increased megakaryocyte count |
|
| C4025272 |
BXGD021615 |
Peripheral arterial stenosis |
|
| C4025731 |
BXGD021763 |
Abnormal thrombosis |
|
| C4048328 |
BXGD021903 |
cervical cancer |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications |
| C4048329 |
BXGD021904 |
Immunosuppression |
|
| C4054188 |
BXGD021977 |
Ph-Like Acute Lymphoblastic Leukemia |
|
| C4086152 |
BXGD022123 |
Childhood Astrocytoma |
Neoplasms |
| C4086165 |
BXGD022126 |
Childhood Neuroblastoma |
Neoplasms |
| C4273671 |
BXGD022333 |
Inherited predisposition to essential thrombocythemia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C4274414 |
BXGD022354 |
Epstein-Barr virus associated gastric carcinoma |
|
| C4303426 |
BXGD022557 |
Refractory anemia with ringed sideroblasts associated with marked thrombocytosis |
Hemic and Lymphatic Diseases |
| C4303761 |
BXGD022567 |
Familial thrombocytosis |
Hemic and Lymphatic Diseases |
| C4324477 |
BXGD022768 |
Transformation to acute myeloid leukaemia |
Neoplasms |
| C4477095 |
BXGD022922 |
Increased lactate dehydrogenase activity |
|
| C4520840 |
BXGD023041 |
Erythroleukemia (Erythroid/Myeloid) |
Neoplasms; Hemic and Lymphatic Diseases |
| C4521042 |
BXGD023055 |
Complete Trisomy 21 Syndrome |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C4525297 |
BXGD023131 |
Stage 0 Gallbladder Cancer AJCC v8 |
|
| C4525300 |
BXGD023132 |
Stage IIA Gallbladder Cancer AJCC v8 |
|
| C4525301 |
BXGD023133 |
Stage IIB Gallbladder Cancer AJCC v8 |
|
| C4525302 |
BXGD023134 |
Stage III Gallbladder Cancer AJCC v8 |
|
| C4525305 |
BXGD023135 |
Stage IV Gallbladder Cancer AJCC v8 |
|
| C4529962 |
BXGD023178 |
Fatty Liver Disease |
|
| C4551637 |
BXGD023379 |
Erythrocytosis familial, 1 |
Hemic and Lymphatic Diseases |
| C4551686 |
BXGD023391 |
Malignant neoplasm of soft tissue |
Neoplasms |
| C4552000 |
BXGD023473 |
Episodic Kinesigenic Dyskinesia 1 |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C4552670 |
BXGD023519 |
Portal Vein Thrombosis, CTCAE |
|
| C4552766 |
BXGD023523 |
Miscarriage |
Female Urogenital Diseases and Pregnancy Complications |
| C4554601 |
BXGD023566 |
Amyloidosis cutis dyschromia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases |
| C4688007 |
BXGD023582 |
Platinum-Resistant Ovarian Carcinoma |
|
| C4721209 |
BXGD023734 |
Metastatic human epidermal growth factor 2 positive carcinoma of breast |
Neoplasms; Skin and Connective Tissue Diseases |
| C4721505 |
BXGD023746 |
Sarcoma, Myeloid |
Neoplasms |
| C4721610 |
BXGD023760 |
Carcinoma, Ovarian Epithelial |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C4721773 |
BXGD023768 |
Postoperative cognitive dysfunction |
|
| C4722085 |
BXGD023788 |
Malignant neoplasm of colon and/or rectum |
|
| C4722518 |
BXGD023806 |
Triple-Negative Breast Carcinoma |
Neoplasms; Skin and Connective Tissue Diseases |
| C4749274 |
BXGD024052 |
Chuvash erythrocytosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C4755296 |
BXGD024091 |
Susceptibility to viral and mycobacterial infection |
|