| C0000768 |
BXGD000007 |
Congenital Abnormality |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C0001339 |
BXGD000041 |
Acute pancreatitis |
Digestive System Diseases |
| C0001418 |
BXGD000050 |
Adenocarcinoma |
Neoplasms |
| C0002395 |
BXGD000111 |
Alzheimer's Disease |
Nervous System Diseases; Mental Disorders |
| C0002418 |
BXGD000112 |
Amblyopia |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C0002736 |
BXGD000127 |
Amyotrophic Lateral Sclerosis |
Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0002793 |
BXGD000130 |
Anaplasia |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0002895 |
BXGD000152 |
Anemia, Sickle Cell |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0002949 |
BXGD000157 |
Aneurysm, Dissecting |
Cardiovascular Diseases |
| C0003123 |
BXGD000178 |
Anorexia |
Pathological Conditions, Signs and Symptoms |
| C0003504 |
BXGD000202 |
Aortic Valve Insufficiency |
Cardiovascular Diseases |
| C0003507 |
BXGD000203 |
Aortic Valve Stenosis |
Cardiovascular Diseases |
| C0003706 |
BXGD000215 |
Arachnodactyly |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0003838 |
BXGD000224 |
Arterial Occlusive Diseases |
Cardiovascular Diseases |
| C0003850 |
BXGD000225 |
Arteriosclerosis |
Cardiovascular Diseases |
| C0003857 |
BXGD000228 |
Congenital arteriovenous malformation |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C0004153 |
BXGD000260 |
Atherosclerosis |
Cardiovascular Diseases |
| C0004352 |
BXGD000269 |
Autistic Disorder |
Mental Disorders |
| C0004903 |
BXGD000293 |
Beckwith-Wiedemann Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C0005586 |
BXGD000315 |
Bipolar Disorder |
Mental Disorders |
| 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 |
| C0006142 |
BXGD000374 |
Malignant neoplasm of breast |
Neoplasms; Skin and Connective Tissue Diseases |
| C0006826 |
BXGD000408 |
Malignant Neoplasms |
Neoplasms |
| C0006849 |
BXGD000413 |
Oral candidiasis |
Infections; Stomatognathic Diseases |
| C0007097 |
BXGD000424 |
Carcinoma |
Neoplasms |
| C0007102 |
BXGD000425 |
Malignant tumor of colon |
Digestive System Diseases; Neoplasms |
| C0007134 |
BXGD000443 |
Renal Cell Carcinoma |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0007222 |
BXGD000454 |
Cardiovascular Diseases |
Cardiovascular Diseases |
| C0007766 |
BXGD000478 |
Intracranial Aneurysm |
Nervous System Diseases; Cardiovascular Diseases |
| C0007785 |
BXGD000485 |
Cerebral Infarction |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases |
| C0008925 |
BXGD000575 |
Cleft Palate |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases |
| 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 |
| C0010054 |
BXGD000647 |
Coronary Arteriosclerosis |
Cardiovascular Diseases |
| C0010068 |
BXGD000648 |
Coronary heart disease |
Cardiovascular Diseases |
| C0011265 |
BXGD000708 |
Presenile dementia |
Nervous System Diseases; Mental Disorders |
| C0011269 |
BXGD000710 |
Dementia, Vascular |
Nervous System Diseases; Mental Disorders; Cardiovascular Diseases |
| C0011303 |
BXGD000712 |
Demyelinating Diseases |
Nervous System Diseases |
| C0011570 |
BXGD000729 |
Mental Depression |
Behavior and Behavior Mechanisms |
| C0011581 |
BXGD000733 |
Depressive disorder |
Mental Disorders |
| C0011603 |
BXGD000734 |
Dermatitis |
Skin and Connective Tissue Diseases |
| C0011847 |
BXGD000749 |
Diabetes |
Endocrine System Diseases |
| C0011849 |
BXGD000751 |
Diabetes Mellitus |
Nutritional and Metabolic Diseases; Endocrine System Diseases |
| C0011860 |
BXGD000755 |
Diabetes Mellitus, Non-Insulin-Dependent |
Nutritional and Metabolic Diseases; Endocrine System Diseases |
| C0013080 |
BXGD000797 |
Down Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0013581 |
BXGD000855 |
Ectopia Lentis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C0014867 |
BXGD000964 |
Esophageal Varices |
Digestive System Diseases |
| C0015672 |
BXGD001011 |
Fatigue |
Pathological Conditions, Signs and Symptoms |
| C0015695 |
BXGD001013 |
Fatty Liver |
Digestive System Diseases |
| C0016412 |
BXGD001058 |
Folic Acid Deficiency |
Nutritional and Metabolic Diseases |
| C0016842 |
BXGD001083 |
Congenital pectus excavatum |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0017181 |
BXGD001103 |
Gastrointestinal Hemorrhage |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C0017574 |
BXGD001122 |
Gingivitis |
Infections; Stomatognathic Diseases |
| C0017601 |
BXGD001125 |
Glaucoma |
Eye Diseases |
| C0017636 |
BXGD001131 |
Glioblastoma |
Neoplasms |
| C0018790 |
BXGD001221 |
Cardiac Arrest |
Cardiovascular Diseases |
| C0018798 |
BXGD001223 |
Congenital Heart Defects |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C0018799 |
BXGD001224 |
Heart Diseases |
Cardiovascular Diseases |
| C0019209 |
BXGD001305 |
Hepatomegaly |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C0019270 |
BXGD001311 |
Hernia |
Pathological Conditions, Signs and Symptoms |
| C0019294 |
BXGD001314 |
Hernia, Inguinal |
Pathological Conditions, Signs and Symptoms |
| C0019569 |
BXGD001337 |
Hirschsprung Disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases |
| C0019880 |
BXGD001351 |
Homocystinuria |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Nervous System Diseases |
| C0020179 |
BXGD001363 |
Huntington Disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders |
| C0020443 |
BXGD001385 |
Hypercholesterolemia |
Nutritional and Metabolic Diseases |
| C0020473 |
BXGD001396 |
Hyperlipidemia |
Nutritional and Metabolic Diseases |
| C0020538 |
BXGD001422 |
Hypertensive disease |
Cardiovascular Diseases |
| C0020550 |
BXGD001429 |
Hyperthyroidism |
Endocrine System Diseases |
| C0021051 |
BXGD001475 |
Immunologic Deficiency Syndromes |
Immune System Diseases |
| C0021390 |
BXGD001503 |
Inflammatory Bowel Diseases |
Digestive System Diseases |
| C0022104 |
BXGD001529 |
Irritable Bowel Syndrome |
Digestive System Diseases |
| C0022336 |
BXGD001535 |
Creutzfeldt-Jakob disease |
Infections; Nervous System Diseases; Mental Disorders |
| C0022821 |
BXGD001590 |
Kyphosis deformity of spine |
Musculoskeletal Diseases |
| C0023316 |
BXGD001633 |
Lens Subluxation |
Eye Diseases |
| 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 |
| C0023462 |
BXGD001654 |
Acute Megakaryocytic Leukemias |
Neoplasms |
| C0023467 |
BXGD001658 |
Leukemia, Myelocytic, Acute |
Neoplasms |
| C0023903 |
BXGD001720 |
Liver neoplasms |
Digestive System Diseases; Neoplasms |
| C0024115 |
BXGD001732 |
Lung diseases |
Respiratory Tract Diseases |
| C0024117 |
BXGD001734 |
Chronic Obstructive Airway Disease |
Respiratory Tract Diseases |
| C0024121 |
BXGD001735 |
Lung Neoplasms |
Neoplasms; Respiratory Tract Diseases |
| C0024302 |
BXGD001760 |
Reticulosarcoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0024304 |
BXGD001762 |
Lymphoma, Mixed-Cell |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0024305 |
BXGD001763 |
Lymphoma, Non-Hodgkin |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0024306 |
BXGD001764 |
Lymphoma, Undifferentiated |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0024534 |
BXGD001784 |
Malaria, Cerebral |
Infections; Nervous System Diseases |
| C0024591 |
BXGD001789 |
Malignant hyperpyrexia due to anesthesia |
Pathological Conditions, Signs and Symptoms |
| C0024623 |
BXGD001791 |
Malignant neoplasm of stomach |
Digestive System Diseases; Neoplasms |
| C0024796 |
BXGD001806 |
Marfan Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases |
| C0025202 |
BXGD001832 |
melanoma |
Neoplasms |
| C0025286 |
BXGD001850 |
Meningioma |
Neoplasms; Nervous System Diseases |
| C0025312 |
BXGD001861 |
Meningomyelocele |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0025362 |
BXGD001866 |
Mental Retardation |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0025517 |
BXGD001875 |
Metabolic Diseases |
Nutritional and Metabolic Diseases |
| C0025521 |
BXGD001876 |
Inborn Errors of Metabolism |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0026267 |
BXGD001896 |
Mitral Valve Prolapse Syndrome |
Cardiovascular Diseases |
| C0026499 |
BXGD001905 |
Monosomy |
Pathological Conditions, Signs and Symptoms |
| C0026946 |
BXGD001951 |
Mycoses |
Infections |
| C0027051 |
BXGD001963 |
Myocardial Infarction |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0027092 |
BXGD001971 |
Myopia |
Eye Diseases |
| C0027627 |
BXGD002006 |
Neoplasm Metastasis |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0027651 |
BXGD002009 |
Neoplasms |
Neoplasms |
| C0027794 |
BXGD002036 |
Neural Tube Defects |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0027819 |
BXGD002043 |
Neuroblastoma |
Neoplasms |
| C0028754 |
BXGD002082 |
Obesity |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases |
| C0029124 |
BXGD002113 |
Optic Atrophy |
Eye Diseases; Nervous System Diseases |
| C0029453 |
BXGD002154 |
Osteopenia |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C0029456 |
BXGD002157 |
Osteoporosis |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C0030305 |
BXGD002206 |
Pancreatitis |
Digestive System Diseases |
| C0030567 |
BXGD002240 |
Parkinson Disease |
Nervous System Diseases |
| C0031099 |
BXGD002282 |
Periodontitis |
Stomatognathic Diseases |
| C0031212 |
BXGD002295 |
Personality Disorders |
Mental Disorders |
| C0031511 |
BXGD002304 |
Pheochromocytoma |
Neoplasms |
| C0032460 |
BXGD002355 |
Polycystic Ovary Syndrome |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C0032580 |
BXGD002362 |
Adenomatous Polyposis Coli |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms |
| C0032617 |
BXGD002367 |
Polyuria |
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0032915 |
BXGD002380 |
Preexcitation Syndrome |
Cardiovascular Diseases |
| C0033975 |
BXGD002447 |
Psychotic Disorders |
Mental Disorders |
| C0034065 |
BXGD002454 |
Pulmonary Embolism |
Respiratory Tract Diseases; Cardiovascular Diseases |
| C0034069 |
BXGD002458 |
Pulmonary Fibrosis |
Respiratory Tract Diseases |
| C0035067 |
BXGD002504 |
Renal Artery Stenosis |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Cardiovascular Diseases |
| C0035305 |
BXGD002529 |
Retinal Detachment |
Eye Diseases |
| C0035328 |
BXGD002537 |
Retinal Vein Occlusion |
Eye Diseases; Cardiovascular Diseases |
| C0036341 |
BXGD002600 |
Schizophrenia |
Mental Disorders |
| C0036439 |
BXGD002615 |
Scoliosis, unspecified |
Musculoskeletal Diseases |
| C0036572 |
BXGD002625 |
Seizures |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0036690 |
BXGD002632 |
Septicemia |
Pathological Conditions, Signs and Symptoms; Infections |
| C0037198 |
BXGD002670 |
Sinus Thrombosis, Intracranial |
Nervous System Diseases; Cardiovascular Diseases |
| C0038454 |
BXGD002760 |
Cerebrovascular accident |
Nervous System Diseases; Cardiovascular Diseases |
| C0038525 |
BXGD002768 |
Subarachnoid Hemorrhage |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases |
| C0038868 |
BXGD002781 |
Progressive supranuclear palsy |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C0040038 |
BXGD002837 |
Thromboembolism |
Cardiovascular Diseases |
| C0040433 |
BXGD002865 |
Tooth Crowding |
Stomatognathic Diseases |
| C0041956 |
BXGD002942 |
Ureteral obstruction |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0042109 |
BXGD002957 |
Urticaria |
Skin and Connective Tissue Diseases; Immune System Diseases |
| C0042373 |
BXGD002978 |
Vascular Diseases |
Cardiovascular Diseases |
| C0042487 |
BXGD002986 |
Venous Thrombosis |
Cardiovascular Diseases |
| C0042693 |
BXGD002996 |
Violence |
|
| C0079740 |
BXGD003088 |
High Grade Lymphoma (neoplasm) |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0079741 |
BXGD003089 |
Lymphoma, Intermediate-Grade |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0079747 |
BXGD003093 |
Low Grade Lymphoma (neoplasm) |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0079757 |
BXGD003095 |
Diffuse Mixed-Cell Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0079770 |
BXGD003098 |
Lymphoma, Small Noncleaved-Cell |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0080178 |
BXGD003107 |
Spina Bifida |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0085648 |
BXGD003221 |
Synovial Cyst |
Neoplasms |
| C0086540 |
BXGD003292 |
Leishmaniasis, New World |
Infections; Skin and Connective Tissue Diseases |
| C0086543 |
BXGD003294 |
Cataract |
Eye Diseases |
| C0149871 |
BXGD003375 |
Deep Vein Thrombosis |
Cardiovascular Diseases |
| C0149939 |
BXGD003390 |
Obstructive nephropathy |
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0151650 |
BXGD003454 |
Renal fibrosis |
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0151699 |
BXGD003461 |
Intracranial Hemorrhage |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases |
| C0151942 |
BXGD003507 |
Arterial thrombosis |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0151945 |
BXGD003508 |
Thrombosis of cerebral veins |
Nervous System Diseases; Cardiovascular Diseases |
| C0152021 |
BXGD003520 |
Congenital heart disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C0153381 |
BXGD003626 |
Malignant neoplasm of mouth |
Neoplasms; Stomatognathic Diseases |
| C0158646 |
BXGD003897 |
Cleft palate with cleft lip |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases |
| C0158731 |
BXGD003902 |
Congenital pectus carinatum |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases |
| C0162298 |
BXGD003933 |
Joint stiffness |
Musculoskeletal Diseases |
| C0162309 |
BXGD003934 |
Adrenoleukodystrophy |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Endocrine System Diseases |
| C0162429 |
BXGD003942 |
Malnutrition |
Nutritional and Metabolic Diseases |
| C0162835 |
BXGD003989 |
Hypopigmentation disorder |
Skin and Connective Tissue Diseases |
| C0206677 |
BXGD004234 |
Adenomatous Polyps |
Neoplasms |
| C0220641 |
BXGD004305 |
Lip and Oral Cavity Carcinoma |
Neoplasms; Stomatognathic Diseases |
| C0231230 |
BXGD004485 |
Fatigability |
|
| C0233514 |
BXGD004584 |
Abnormal behavior |
Behavior and Behavior Mechanisms |
| C0234985 |
BXGD004708 |
Mental deterioration |
Mental Disorders |
| C0240635 |
BXGD005047 |
Byzanthine arch palate |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Stomatognathic Diseases |
| C0241240 |
BXGD005089 |
Tall stature |
|
| C0242379 |
BXGD005157 |
Malignant neoplasm of lung |
Neoplasms; Respiratory Tract Diseases |
| C0243026 |
BXGD005210 |
Sepsis |
Pathological Conditions, Signs and Symptoms; Infections |
| C0263401 |
BXGD005298 |
Cutis marmorata |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Skin and Connective Tissue Diseases; Cardiovascular Diseases; Wounds and Injuries |
| C0263490 |
BXGD005314 |
Brittle hair |
|
| C0268009 |
BXGD005801 |
Hyperosmolality |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Nervous System Diseases |
| C0268621 |
BXGD006012 |
Hepatic methionine adenosyltransferase deficiency |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0278878 |
BXGD006609 |
Adult Glioblastoma |
Neoplasms |
| C0279702 |
BXGD006685 |
Conventional (Clear Cell) Renal Cell Carcinoma |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0280474 |
BXGD006748 |
Childhood Glioblastoma |
Neoplasms |
| C0282193 |
BXGD006798 |
Iron Overload |
Nutritional and Metabolic Diseases |
| C0302142 |
BXGD006831 |
Deformity |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C0338451 |
BXGD007176 |
Frontotemporal dementia |
Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders |
| C0338474 |
BXGD007183 |
Central nervous system demyelination |
|
| C0338573 |
BXGD007199 |
Cerebral venous sinus thrombosis |
Nervous System Diseases; Cardiovascular Diseases |
| C0338656 |
BXGD007211 |
Impaired cognition |
Mental Disorders |
| C0338715 |
BXGD007213 |
Drug-induced depressive state |
Chemically-Induced Disorders; Mental Disorders |
| C0344315 |
BXGD007666 |
Depressed mood |
Behavior and Behavior Mechanisms |
| C0345392 |
BXGD007732 |
Congenital kyphoscoliosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0373721 |
BXGD007965 |
Selenium measurement |
|
| C0374997 |
BXGD007967 |
Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site |
|
| C0375206 |
BXGD007973 |
Hemiplegia/hemiparesis |
|
| C0376358 |
BXGD007992 |
Malignant neoplasm of prostate |
Neoplasms; Male Urogenital Diseases |
| C0376705 |
BXGD008009 |
Viral Load result |
|
| C0398623 |
BXGD008202 |
Thrombophilia |
Hemic and Lymphatic Diseases |
| C0424295 |
BXGD008524 |
Hyperactive behavior |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0432283 |
BXGD008764 |
Osteoglophonic dwarfism |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0497327 |
BXGD009061 |
Dementia |
Nervous System Diseases; Mental Disorders |
| C0524851 |
BXGD009246 |
Neurodegenerative Disorders |
Nervous System Diseases |
| C0557874 |
BXGD009444 |
Global developmental delay |
|
| C0559106 |
BXGD009465 |
Ventricular preexcitation |
Pathological Conditions, Signs and Symptoms |
| C0575158 |
BXGD009515 |
Kyphoscoliosis deformity of spine |
Musculoskeletal Diseases |
| C0576093 |
BXGD009525 |
Knee joint valgus deformity |
Musculoskeletal 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 |
| C0598608 |
BXGD009668 |
Hyperhomocysteinemia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0598766 |
BXGD009669 |
Leukemogenesis |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0600033 |
BXGD009682 |
Acquired Kyphoscoliosis |
Musculoskeletal Diseases |
| C0600139 |
BXGD009695 |
Prostate carcinoma |
Neoplasms; Male Urogenital Diseases |
| C0678222 |
BXGD009749 |
Breast Carcinoma |
Neoplasms; Skin and Connective Tissue Diseases |
| C0684249 |
BXGD009790 |
Carcinoma of lung |
Neoplasms; Respiratory Tract Diseases |
| C0685938 |
BXGD009829 |
Malignant neoplasm of gastrointestinal tract |
Digestive System Diseases; Neoplasms |
| C0699753 |
BXGD009864 |
Cancer Relapse |
|
| 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 |
| C0740391 |
BXGD009987 |
Middle Cerebral Artery Occlusion |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases |
| C0751074 |
BXGD010313 |
Diabetic Neuralgia |
Nervous System Diseases; Endocrine System Diseases |
| C0751202 |
BXGD010347 |
Cystathionine beta-Synthase Deficiency Disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Nervous System Diseases |
| C0751606 |
BXGD010523 |
Adult Acute Lymphocytic Leukemia |
|
| C0751967 |
BXGD010657 |
Multiple Sclerosis, Relapsing-Remitting |
Immune System Diseases; Nervous System Diseases |
| C0752304 |
BXGD010711 |
Hypoxic-Ischemic Encephalopathy |
Nervous System Diseases; Cardiovascular Diseases |
| C0810364 |
BXGD010846 |
Cleft Lip with or without Cleft Palate |
|
| C0852949 |
BXGD010957 |
Arteriopathic disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0854107 |
BXGD010999 |
Subcutaneous hemorrhage |
Skin and Connective Tissue Diseases |
| C0856169 |
BXGD011096 |
Endothelial dysfunction |
|
| C0917798 |
BXGD011409 |
Cerebral Ischemia |
Nervous System Diseases; Cardiovascular Diseases |
| C0919267 |
BXGD011426 |
ovarian neoplasm |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C0936215 |
BXGD011476 |
Vitamin B 6 Deficiency |
Nutritional and Metabolic Diseases |
| C0948008 |
BXGD011499 |
Ischemic stroke |
Nervous System Diseases; Cardiovascular Diseases |
| C1140680 |
BXGD011718 |
Malignant neoplasm of ovary |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C1168401 |
BXGD011792 |
Squamous cell carcinoma of the head and neck |
Neoplasms |
| C1258666 |
BXGD011825 |
Myxoid cyst |
Neoplasms; Skin and Connective Tissue Diseases |
| C1260403 |
BXGD011832 |
prothrombin gene mutation |
Hemic and Lymphatic Diseases |
| C1263846 |
BXGD011897 |
Attention deficit hyperactivity disorder |
Mental Disorders |
| C1269955 |
BXGD012005 |
Tumor Cell Invasion |
|
| C1270972 |
BXGD012006 |
Mild cognitive disorder |
Mental Disorders |
| C1306459 |
BXGD012361 |
Primary malignant neoplasm |
Neoplasms |
| C1306460 |
BXGD012362 |
Primary malignant neoplasm of lung |
Neoplasms; Respiratory Tract Diseases |
| C1328440 |
BXGD012466 |
Abnormality of amino acid metabolism |
|
| C1332977 |
BXGD012569 |
Childhood Leukemia |
Neoplasms |
| C1536500 |
BXGD013345 |
Deficiency of acetyl-CoA acetyltransferase |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C1561643 |
BXGD013363 |
Chronic Kidney Diseases |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C1565489 |
BXGD013401 |
Renal Insufficiency |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C1621958 |
BXGD013468 |
Glioblastoma Multiforme |
Neoplasms |
| C1704436 |
BXGD013564 |
Peripheral Arterial Diseases |
Cardiovascular Diseases |
| C1836230 |
BXGD014099 |
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO |
|
| C1836231 |
BXGD014100 |
HIV-1, RESISTANCE TO |
|
| C1836232 |
BXGD014101 |
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO |
|
| C1836233 |
BXGD014102 |
AIDS, PROGRESSION TO |
|
| C1836996 |
BXGD014183 |
Disproportionate tall stature |
|
| C1837218 |
BXGD014207 |
Cleft palate, isolated |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases |
| C1848701 |
BXGD014967 |
Elevated hepatic transaminase |
|
| C1856087 |
BXGD015571 |
Biconcave vertebral bodies |
|
| C1856089 |
BXGD015572 |
Methioninuria |
|
| C1857042 |
BXGD015669 |
Sparse scalp hair |
|
| C1857108 |
BXGD015677 |
Limitation of joint mobility |
|
| C1861537 |
BXGD016058 |
OROFACIAL CLEFT 1 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases |
| C1862475 |
BXGD016132 |
Abnormality of retinal pigmentation |
|
| C1867743 |
BXGD016470 |
Premature coronary artery atherosclerosis |
Cardiovascular Diseases |
| C1956346 |
BXGD016627 |
Coronary Artery Disease |
Cardiovascular Diseases |
| C1963943 |
BXGD016706 |
Atherothrombosis |
|
| C1969372 |
BXGD016775 |
Tubulointerstitial fibrosis |
|
| C2239176 |
BXGD016965 |
Liver carcinoma |
Digestive System Diseases; Neoplasms |
| C2242817 |
BXGD017005 |
Homocysteine measurement |
|
| C2363725 |
BXGD017098 |
Arthrosclerosis |
|
| C2678065 |
BXGD017398 |
Myofibrillar Myopathy |
Musculoskeletal Diseases; Nervous System Diseases |
| C2711227 |
BXGD017478 |
Steatohepatitis |
Digestive System Diseases |
| C2826323 |
BXGD017790 |
Refractory Cytopenia of Childhood |
|
| C2981150 |
BXGD018211 |
Uranostaphyloschisis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases |
| C3150344 |
BXGD018302 |
HYPERHOMOCYSTEINEMIA, THROMBOTIC, CBS-RELATED |
|
| C3495426 |
BXGD018983 |
Homocysteinemia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C3502110 |
BXGD019040 |
Homocystinuria, Pyridoxine-Responsive |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Nervous System Diseases |
| C3714542 |
BXGD019413 |
Lymphoma, Diffuse |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C3714756 |
BXGD019429 |
Intellectual Disability |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C3714941 |
BXGD019439 |
OTOFACIOCERVICAL SYNDROME 1 |
|
| C3805043 |
BXGD019457 |
Vascular cognitive impairment |
|
| C3805574 |
BXGD019481 |
Increased fracture rate |
|
| C3806347 |
BXGD019506 |
Hyperhomocystinemia |
|
| C4017308 |
BXGD020437 |
HOMOCYSTINURIA, PYRIDOXINE-NONRESPONSIVE |
|
| C4021813 |
BXGD020799 |
Oral cleft |
|
| C4048705 |
BXGD021907 |
Hypermethioninemia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C4086165 |
BXGD022126 |
Childhood Neuroblastoma |
Neoplasms |
| C4521042 |
BXGD023055 |
Complete Trisomy 21 Syndrome |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C4551680 |
BXGD023387 |
Generalized osteoporosis |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C4551683 |
BXGD023389 |
Adrenal Gland Pheochromocytoma |
Neoplasms; Endocrine System Diseases |
| C4688007 |
BXGD023582 |
Platinum-Resistant Ovarian Carcinoma |
|
| C4707243 |
BXGD023712 |
Familial thoracic aortic aneurysm and aortic dissection |
|
| C4721532 |
BXGD023752 |
Lymphoma, Non-Hodgkin, Familial |
Neoplasms; Immune System Diseases; Hemic and Lymphatic 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 |
|
