| C0000768 |
BXGD000007 |
Congenital Abnormality |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C0000786 |
BXGD000010 |
Spontaneous abortion |
Female Urogenital Diseases and Pregnancy Complications |
| C0000809 |
BXGD000011 |
Abortion, Habitual |
Female Urogenital Diseases and Pregnancy Complications |
| C0000832 |
BXGD000013 |
Abruptio Placentae |
Female Urogenital Diseases and Pregnancy Complications |
| C0001206 |
BXGD000033 |
Acromegaly |
Musculoskeletal Diseases; Nervous System Diseases; Endocrine System Diseases |
| C0001403 |
BXGD000048 |
Addison Disease |
Immune System Diseases; Endocrine System Diseases |
| C0001418 |
BXGD000050 |
Adenocarcinoma |
Neoplasms |
| C0001430 |
BXGD000054 |
Adenoma |
Neoplasms |
| C0001723 |
BXGD000071 |
Affective Disorders, Psychotic |
Mental Disorders |
| C0001787 |
BXGD000076 |
Osteoporosis, Age-Related |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C0001857 |
BXGD000085 |
AIDS related complex |
Infections; Immune System Diseases |
| C0001948 |
BXGD000091 |
Alcohol consumption |
Behavior and Behavior Mechanisms |
| C0001956 |
BXGD000092 |
Alcohol Use Disorder |
Chemically-Induced Disorders; Mental Disorders |
| C0001969 |
BXGD000094 |
Alcoholic Intoxication |
Chemically-Induced Disorders; Mental Disorders |
| C0001973 |
BXGD000095 |
Alcoholic Intoxication, Chronic |
Chemically-Induced Disorders; Mental Disorders |
| C0002170 |
BXGD000105 |
Alopecia |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases |
| C0002171 |
BXGD000106 |
Alopecia Areata |
Skin and Connective Tissue Diseases |
| C0002312 |
BXGD000107 |
alpha-Thalassemia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0002395 |
BXGD000111 |
Alzheimer's Disease |
Nervous System Diseases; Mental Disorders |
| C0002622 |
BXGD000119 |
Amnesia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0002736 |
BXGD000127 |
Amyotrophic Lateral Sclerosis |
Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0002871 |
BXGD000132 |
Anemia |
Hemic and Lymphatic Diseases |
| C0002875 |
BXGD000135 |
Cooley's anemia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0002878 |
BXGD000137 |
Anemia, Hemolytic |
Hemic and Lymphatic Diseases |
| C0002888 |
BXGD000145 |
Anemia, Megaloblastic |
Hemic and Lymphatic Diseases |
| C0002895 |
BXGD000152 |
Anemia, Sickle Cell |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0002902 |
BXGD000154 |
Anencephaly |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0002949 |
BXGD000157 |
Aneurysm, Dissecting |
Cardiovascular Diseases |
| C0003467 |
BXGD000194 |
Anxiety |
Behavior and Behavior Mechanisms |
| C0003469 |
BXGD000195 |
Anxiety Disorders |
Mental Disorders |
| C0003838 |
BXGD000224 |
Arterial Occlusive Diseases |
Cardiovascular Diseases |
| C0003850 |
BXGD000225 |
Arteriosclerosis |
Cardiovascular Diseases |
| C0003855 |
BXGD000227 |
Arteriovenous fistula |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C0003864 |
BXGD000231 |
Arthritis |
Musculoskeletal Diseases |
| C0003872 |
BXGD000235 |
Arthritis, Psoriatic |
Skin and Connective Tissue Diseases; Musculoskeletal Diseases |
| C0003873 |
BXGD000236 |
Rheumatoid Arthritis |
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases |
| C0004096 |
BXGD000252 |
Asthma |
Respiratory Tract Diseases; Immune System Diseases |
| C0004135 |
BXGD000257 |
Ataxia Telangiectasia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases; Nervous System Diseases; Cardiovascular Diseases |
| C0004153 |
BXGD000260 |
Atherosclerosis |
Cardiovascular Diseases |
| C0004238 |
BXGD000262 |
Atrial Fibrillation |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0004352 |
BXGD000269 |
Autistic Disorder |
Mental Disorders |
| C0004364 |
BXGD000270 |
Autoimmune Diseases |
Immune System Diseases |
| C0004509 |
BXGD000275 |
Azoospermia |
Male Urogenital Diseases |
| C0004763 |
BXGD000289 |
Barrett Esophagus |
Digestive System Diseases; Neoplasms |
| C0004903 |
BXGD000293 |
Beckwith-Wiedemann Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C0004936 |
BXGD000295 |
Mental disorders |
Mental Disorders |
| C0004943 |
BXGD000297 |
Behcet Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases |
| C0005586 |
BXGD000315 |
Bipolar Disorder |
Mental Disorders |
| C0005587 |
BXGD000316 |
Depression, Bipolar |
Mental Disorders |
| C0005612 |
BXGD000317 |
Birth Weight |
Pathological Conditions, Signs and Symptoms |
| 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 |
| C0005779 |
BXGD000336 |
Blood Coagulation Disorders |
Hemic and Lymphatic Diseases |
| C0005823 |
BXGD000339 |
Blood Pressure |
|
| C0005956 |
BXGD000356 |
Bone Marrow Diseases |
Hemic and Lymphatic Diseases |
| C0006012 |
BXGD000360 |
Borderline Personality Disorder |
Mental Disorders |
| C0006118 |
BXGD000372 |
Brain Neoplasms |
Neoplasms; Nervous System Diseases |
| C0006142 |
BXGD000374 |
Malignant neoplasm of breast |
Neoplasms; Skin and Connective Tissue Diseases |
| C0006287 |
BXGD000390 |
Bronchopulmonary Dysplasia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases |
| C0006826 |
BXGD000408 |
Malignant Neoplasms |
Neoplasms |
| C0007097 |
BXGD000424 |
Carcinoma |
Neoplasms |
| C0007102 |
BXGD000425 |
Malignant tumor of colon |
Digestive System Diseases; Neoplasms |
| C0007103 |
BXGD000426 |
Malignant neoplasm of endometrium |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications |
| C0007107 |
BXGD000428 |
Malignant neoplasm of larynx |
Neoplasms; Respiratory Tract Diseases; Otorhinolaryngologic Diseases |
| C0007113 |
BXGD000430 |
Rectal Carcinoma |
Digestive System Diseases; Neoplasms |
| C0007114 |
BXGD000431 |
Malignant neoplasm of skin |
Neoplasms; Skin and Connective Tissue Diseases |
| C0007115 |
BXGD000432 |
Malignant neoplasm of thyroid |
Neoplasms; Endocrine System Diseases |
| 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 |
| C0007138 |
BXGD000446 |
Carcinoma, Transitional Cell |
Neoplasms |
| C0007222 |
BXGD000454 |
Cardiovascular Diseases |
Cardiovascular Diseases |
| C0007273 |
BXGD000455 |
Carotid Artery Diseases |
Nervous System Diseases; Cardiovascular Diseases |
| C0007282 |
BXGD000458 |
Carotid Stenosis |
Nervous System Diseases; Cardiovascular Diseases |
| C0007570 |
BXGD000467 |
Celiac Disease |
Digestive System Diseases; Nutritional and Metabolic Diseases |
| C0007688 |
BXGD000473 |
Central Retinal Artery Occlusion |
Eye Diseases; Cardiovascular Diseases |
| C0007766 |
BXGD000478 |
Intracranial Aneurysm |
Nervous System Diseases; Cardiovascular Diseases |
| C0007775 |
BXGD000482 |
Cerebral Atherosclerosis |
Nervous System Diseases; Cardiovascular Diseases |
| C0007785 |
BXGD000485 |
Cerebral Infarction |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases |
| C0007786 |
BXGD000486 |
Brain Ischemia |
Nervous System Diseases; Cardiovascular Diseases |
| C0007787 |
BXGD000487 |
Transient Ischemic Attack |
Nervous System Diseases; Cardiovascular Diseases |
| C0007789 |
BXGD000488 |
Cerebral Palsy |
Nervous System Diseases |
| C0007820 |
BXGD000491 |
Cerebrovascular Disorders |
Nervous System Diseases; Cardiovascular Diseases |
| C0007847 |
BXGD000492 |
Malignant tumor of cervix |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications |
| C0007868 |
BXGD000498 |
Cervical dysplasia |
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 |
| C0008073 |
BXGD000518 |
Developmental Disabilities |
Mental Disorders |
| C0008479 |
BXGD000544 |
Chondrosarcoma |
Neoplasms |
| C0008626 |
BXGD000559 |
Congenital chromosomal disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C0008924 |
BXGD000574 |
Cleft upper lip |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases |
| C0008925 |
BXGD000575 |
Cleft Palate |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases |
| C0009081 |
BXGD000581 |
Congenital clubfoot |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0009088 |
BXGD000585 |
Cluster Headache |
Nervous System Diseases |
| C0009319 |
BXGD000596 |
Colitis |
Digestive System Diseases |
| C0009324 |
BXGD000597 |
Ulcerative Colitis |
Digestive System Diseases |
| C0009375 |
BXGD000602 |
Colonic Neoplasms |
Digestive System Diseases; Neoplasms |
| C0009402 |
BXGD000605 |
Colorectal Carcinoma |
Digestive System Diseases; Neoplasms |
| C0009404 |
BXGD000606 |
Colorectal Neoplasms |
Digestive System Diseases; Neoplasms |
| C0010054 |
BXGD000647 |
Coronary Arteriosclerosis |
Cardiovascular Diseases |
| C0010068 |
BXGD000648 |
Coronary heart disease |
Cardiovascular Diseases |
| C0010346 |
BXGD000664 |
Crohn Disease |
Digestive System Diseases |
| C0010823 |
BXGD000690 |
Cytomegalovirus Infections |
Infections |
| C0011057 |
BXGD000695 |
Hearing Loss, Sudden |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases |
| C0011253 |
BXGD000706 |
Delusions |
Behavior and Behavior Mechanisms |
| C0011265 |
BXGD000708 |
Presenile dementia |
Nervous System Diseases; Mental Disorders |
| C0011268 |
BXGD000709 |
Senile dementia |
Nervous System Diseases; Mental Disorders |
| C0011269 |
BXGD000710 |
Dementia, Vascular |
Nervous System Diseases; Mental Disorders; Cardiovascular Diseases |
| C0011570 |
BXGD000729 |
Mental Depression |
Behavior and Behavior Mechanisms |
| C0011573 |
BXGD000730 |
Endogenous depression |
Mental Disorders |
| C0011581 |
BXGD000733 |
Depressive disorder |
Mental Disorders |
| C0011609 |
BXGD000737 |
Drug Eruptions |
Skin and Connective Tissue Diseases; Immune System Diseases; Chemically-Induced Disorders |
| 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 |
| C0011853 |
BXGD000752 |
Diabetes Mellitus, Experimental |
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 |
| C0011875 |
BXGD000757 |
Diabetic Angiopathies |
Endocrine System Diseases; Cardiovascular Diseases |
| C0011881 |
BXGD000760 |
Diabetic Nephropathy |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases |
| C0011882 |
BXGD000761 |
Diabetic Neuropathies |
Nervous System Diseases; Endocrine System Diseases |
| C0011884 |
BXGD000762 |
Diabetic Retinopathy |
Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases |
| C0011991 |
BXGD000766 |
Diarrhea |
Pathological Conditions, Signs and Symptoms |
| C0011999 |
BXGD000770 |
Diastematomyelia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0013080 |
BXGD000797 |
Down Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0013146 |
BXGD000801 |
Drug abuse |
Chemically-Induced Disorders; Mental Disorders |
| C0013170 |
BXGD000802 |
Drug habituation |
Chemically-Induced Disorders; Mental Disorders |
| C0013221 |
BXGD000804 |
Drug toxicity |
Chemically-Induced Disorders |
| C0013238 |
BXGD000806 |
Dry Eye Syndromes |
Eye Diseases |
| C0013274 |
BXGD000809 |
Patent ductus arteriosus |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C0013404 |
BXGD000833 |
Dyspnea |
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases |
| C0013537 |
BXGD000853 |
Eclampsia |
Female Urogenital Diseases and Pregnancy Complications |
| C0013595 |
BXGD000858 |
Eczema |
Skin and Connective Tissue Diseases |
| C0014068 |
BXGD000886 |
Encephalomalacia |
Nervous System Diseases |
| C0014170 |
BXGD000902 |
Endometrial Neoplasms |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications |
| C0014457 |
BXGD000915 |
Eosinophilia |
Hemic and Lymphatic Diseases |
| C0014544 |
BXGD000926 |
Epilepsy |
Nervous System Diseases |
| C0014670 |
BXGD000941 |
Equinus Deformity |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0014772 |
BXGD000948 |
Red Blood Cell Count measurement |
|
| C0014859 |
BXGD000961 |
Esophageal Neoplasms |
Digestive System Diseases; Neoplasms |
| C0014869 |
BXGD000966 |
Peptic Esophagitis |
Digestive System 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 |
| C0015702 |
BXGD001016 |
Favism |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Chemically-Induced Disorders; Hemic and Lymphatic Diseases |
| C0015934 |
BXGD001026 |
Fetal Growth Retardation |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications |
| C0015967 |
BXGD001030 |
Fever |
Pathological Conditions, Signs and Symptoms |
| C0016034 |
BXGD001034 |
Breast Fibrocystic Disease |
Skin and Connective Tissue Diseases |
| C0016053 |
BXGD001041 |
Fibromyalgia |
Musculoskeletal Diseases; Nervous System Diseases |
| C0016412 |
BXGD001058 |
Folic Acid Deficiency |
Nutritional and Metabolic Diseases |
| C0016522 |
BXGD001067 |
Foramen Ovale, Patent |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C0017178 |
BXGD001102 |
Gastrointestinal Diseases |
Digestive System Diseases |
| C0017205 |
BXGD001105 |
Gaucher Disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0017601 |
BXGD001125 |
Glaucoma |
Eye Diseases |
| C0017605 |
BXGD001126 |
Angle Closure Glaucoma |
Eye Diseases |
| C0017606 |
BXGD001127 |
Primary angle-closure glaucoma |
Eye Diseases |
| C0017612 |
BXGD001129 |
Glaucoma, Open-Angle |
Eye Diseases |
| C0017636 |
BXGD001131 |
Glioblastoma |
Neoplasms |
| C0017638 |
BXGD001132 |
Glioma |
Neoplasms |
| C0017665 |
BXGD001141 |
Membranous glomerulonephritis |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases |
| C0017668 |
BXGD001143 |
Focal glomerulosclerosis |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0018081 |
BXGD001171 |
Gonorrhea |
Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases |
| C0018133 |
BXGD001176 |
Graft-vs-Host Disease |
Immune System Diseases |
| C0018213 |
BXGD001187 |
Graves Disease |
Eye Diseases; Immune System Diseases; Endocrine System Diseases |
| C0018524 |
BXGD001200 |
Hallucinations |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms |
| C0018681 |
BXGD001214 |
Headache |
Pathological Conditions, Signs and Symptoms |
| C0018784 |
BXGD001220 |
Sensorineural Hearing Loss (disorder) |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases |
| 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 |
| C0018802 |
BXGD001227 |
Congestive heart failure |
Cardiovascular Diseases |
| C0018817 |
BXGD001235 |
Atrial Septal Defects |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C0018818 |
BXGD001236 |
Ventricular Septal Defects |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C0018939 |
BXGD001253 |
Hematological Disease |
Hemic and Lymphatic Diseases |
| C0018965 |
BXGD001258 |
Hematuria |
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0019034 |
BXGD001268 |
Hemoglobin SC Disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0019061 |
BXGD001273 |
Hemolytic-Uremic Syndrome |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Hemic and Lymphatic Diseases |
| C0019069 |
BXGD001277 |
Hemophilia A |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0019154 |
BXGD001291 |
Hepatic Vein Thrombosis |
Digestive System Diseases; Cardiovascular Diseases |
| C0019156 |
BXGD001292 |
Hepatic Veno-Occlusive Disease |
Digestive System Diseases; Cardiovascular Diseases |
| C0019158 |
BXGD001293 |
Hepatitis |
Digestive System Diseases |
| C0019159 |
BXGD001294 |
Hepatitis A |
Digestive System Diseases; Infections |
| C0019163 |
BXGD001295 |
Hepatitis B |
Digestive System Diseases; Infections |
| C0019193 |
BXGD001299 |
Hepatitis, Toxic |
Digestive System Diseases; Chemically-Induced Disorders |
| C0019196 |
BXGD001301 |
Hepatitis C |
Digestive System Diseases; Infections |
| C0019202 |
BXGD001302 |
Hepatolenticular Degeneration |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0019829 |
BXGD001350 |
Hodgkin Disease |
Neoplasms; Immune System Diseases; Hemic and Lymphatic 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 |
| C0020433 |
BXGD001379 |
Hyperbilirubinemia |
Pathological Conditions, Signs and Symptoms |
| C0020443 |
BXGD001385 |
Hypercholesterolemia |
Nutritional and Metabolic Diseases |
| C0020445 |
BXGD001386 |
Hypercholesterolemia, Familial |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0020456 |
BXGD001392 |
Hyperglycemia |
Nutritional and Metabolic Diseases |
| C0020473 |
BXGD001396 |
Hyperlipidemia |
Nutritional and Metabolic Diseases |
| C0020476 |
BXGD001398 |
Hyperlipoproteinemias |
Nutritional and Metabolic Diseases |
| C0020502 |
BXGD001410 |
Hyperparathyroidism |
Endocrine System Diseases |
| C0020517 |
BXGD001415 |
Hypersensitivity |
Immune System Diseases |
| C0020538 |
BXGD001422 |
Hypertensive disease |
Cardiovascular Diseases |
| C0020550 |
BXGD001429 |
Hyperthyroidism |
Endocrine System Diseases |
| C0020557 |
BXGD001432 |
Hypertriglyceridemia |
Nutritional and Metabolic Diseases |
| C0020615 |
BXGD001445 |
Hypoglycemia |
Nutritional and Metabolic Diseases |
| C0020676 |
BXGD001462 |
Hypothyroidism |
Endocrine System Diseases |
| C0021308 |
BXGD001494 |
Infarction |
Pathological Conditions, Signs and Symptoms |
| C0021361 |
BXGD001499 |
Female infertility |
Female Urogenital Diseases and Pregnancy Complications |
| C0021364 |
BXGD001500 |
Male infertility |
Male Urogenital Diseases |
| C0021390 |
BXGD001503 |
Inflammatory Bowel Diseases |
Digestive System Diseases |
| C0021775 |
BXGD001512 |
Intermittent Claudication |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0022104 |
BXGD001529 |
Irritable Bowel Syndrome |
Digestive System Diseases |
| C0022658 |
BXGD001570 |
Kidney Diseases |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0022660 |
BXGD001571 |
Kidney Failure, Acute |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0022661 |
BXGD001572 |
Kidney Failure, Chronic |
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 |
| C0023234 |
BXGD001622 |
Legg-Calve-Perthes Disease |
Musculoskeletal Diseases |
| C0023418 |
BXGD001642 |
leukemia |
Neoplasms |
| C0023434 |
BXGD001643 |
Chronic Lymphocytic Leukemia |
Neoplasms; Immune System Diseases; 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 |
| C0023453 |
BXGD001652 |
L2 Acute Lymphoblastic Leukemia |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| 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 |
| C0023493 |
BXGD001672 |
Adult T-Cell Lymphoma/Leukemia |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0023530 |
BXGD001683 |
Leukopenia |
Hemic and Lymphatic Diseases |
| C0023646 |
BXGD001690 |
Lichen Planus |
Skin and Connective Tissue Diseases |
| C0023787 |
BXGD001698 |
Lipodystrophy |
Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases |
| C0023890 |
BXGD001713 |
Liver Cirrhosis |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C0023891 |
BXGD001714 |
Liver Cirrhosis, Alcoholic |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Chemically-Induced Disorders |
| C0023895 |
BXGD001717 |
Liver diseases |
Digestive System Diseases |
| C0023903 |
BXGD001720 |
Liver neoplasms |
Digestive System Diseases; Neoplasms |
| C0024121 |
BXGD001735 |
Lung Neoplasms |
Neoplasms; Respiratory Tract Diseases |
| C0024131 |
BXGD001736 |
Lupus Vulgaris |
Infections; Skin and Connective Tissue Diseases |
| C0024138 |
BXGD001738 |
Lupus Erythematosus, Discoid |
Skin and Connective Tissue 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 |
| C0024301 |
BXGD001759 |
Lymphoma, Follicular |
Neoplasms; Immune System Diseases; Hemic and Lymphatic 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 |
| C0024314 |
BXGD001767 |
Lymphoproliferative Disorders |
Immune System Diseases; Hemic and Lymphatic Diseases |
| C0024530 |
BXGD001783 |
Malaria |
Infections |
| C0024620 |
BXGD001790 |
Primary Malignant Liver Neoplasm |
Digestive System Diseases; Neoplasms |
| C0024623 |
BXGD001791 |
Malignant neoplasm of stomach |
Digestive System Diseases; Neoplasms |
| C0024713 |
BXGD001799 |
Manic Disorder |
Mental Disorders |
| C0024796 |
BXGD001806 |
Marfan Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases |
| C0024814 |
BXGD001809 |
Marinesco-Sjogren syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0025193 |
BXGD001831 |
Melancholia |
Mental Disorders |
| C0025281 |
BXGD001848 |
Meniere Disease |
Otorhinolaryngologic Diseases |
| C0025286 |
BXGD001850 |
Meningioma |
Neoplasms; Nervous System Diseases |
| C0025312 |
BXGD001861 |
Meningomyelocele |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0025322 |
BXGD001863 |
Premature Menopause |
Female Urogenital Diseases and Pregnancy Complications |
| 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 |
| C0025945 |
BXGD001881 |
Microangiopathy, Diabetic |
Endocrine System Diseases; Cardiovascular Diseases |
| C0025958 |
BXGD001882 |
Microcephaly |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases |
| C0026654 |
BXGD001914 |
Moyamoya Disease |
Nervous System Diseases; Cardiovascular 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 |
| C0026918 |
BXGD001948 |
Mycobacterium Infections |
Infections |
| C0027051 |
BXGD001963 |
Myocardial Infarction |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0027497 |
BXGD001993 |
Nausea |
Pathological Conditions, Signs and Symptoms |
| C0027540 |
BXGD001996 |
Necrosis |
Pathological Conditions, Signs and Symptoms |
| C0027543 |
BXGD001997 |
Avascular necrosis of bone |
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases |
| C0027562 |
BXGD001999 |
Negativism |
Behavior and Behavior Mechanisms |
| 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 |
| C0027726 |
BXGD002030 |
Nephrotic Syndrome |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0027765 |
BXGD002033 |
nervous system disorder |
Nervous System Diseases |
| C0027794 |
BXGD002036 |
Neural Tube Defects |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0027806 |
BXGD002039 |
Neurenteric Cyst |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0027819 |
BXGD002043 |
Neuroblastoma |
Neoplasms |
| C0027947 |
BXGD002061 |
Neutropenia |
Hemic and Lymphatic Diseases |
| C0028754 |
BXGD002082 |
Obesity |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases |
| C0028768 |
BXGD002084 |
Obsessive-Compulsive Disorder |
Mental Disorders |
| C0028960 |
BXGD002101 |
Oligospermia |
Male Urogenital Diseases |
| C0029408 |
BXGD002137 |
Degenerative polyarthritis |
Musculoskeletal Diseases |
| C0029445 |
BXGD002153 |
Bone necrosis |
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases |
| C0029453 |
BXGD002154 |
Osteopenia |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C0029456 |
BXGD002157 |
Osteoporosis |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C0029463 |
BXGD002160 |
Osteosarcoma |
Neoplasms |
| C0030193 |
BXGD002191 |
Pain |
Pathological Conditions, Signs and Symptoms |
| C0030297 |
BXGD002204 |
Pancreatic Neoplasm |
Digestive System Diseases; Neoplasms; Endocrine System Diseases |
| C0030554 |
BXGD002239 |
Paresthesia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0030567 |
BXGD002240 |
Parkinson Disease |
Nervous System Diseases |
| C0031117 |
BXGD002285 |
Peripheral Neuropathy |
Nervous System Diseases |
| C0032460 |
BXGD002355 |
Polycystic Ovary Syndrome |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C0032463 |
BXGD002357 |
Polycythemia Vera |
Neoplasms; Hemic and Lymphatic Diseases |
| C0032580 |
BXGD002362 |
Adenomatous Polyposis Coli |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms |
| C0032584 |
BXGD002363 |
polyps |
Pathological Conditions, Signs and Symptoms |
| C0032914 |
BXGD002379 |
Pre-Eclampsia |
Female Urogenital Diseases and Pregnancy Complications |
| C0032962 |
BXGD002382 |
Pregnancy Complications |
Female Urogenital Diseases and Pregnancy Complications |
| C0032969 |
BXGD002385 |
Pregnancy in Diabetics |
Female Urogenital Diseases and Pregnancy Complications |
| C0033246 |
BXGD002401 |
Proctitis |
Digestive System Diseases |
| C0033578 |
BXGD002408 |
Prostatic Neoplasms |
Neoplasms; Male Urogenital Diseases |
| C0033626 |
BXGD002412 |
Protein Deficiency |
Nutritional and Metabolic Diseases |
| C0033860 |
BXGD002438 |
Psoriasis |
Skin and Connective Tissue Diseases |
| C0033975 |
BXGD002447 |
Psychotic Disorders |
Mental Disorders |
| C0034065 |
BXGD002454 |
Pulmonary Embolism |
Respiratory Tract Diseases; Cardiovascular Diseases |
| C0034152 |
BXGD002467 |
Henoch-Schoenlein Purpura |
Pathological Conditions, Signs and Symptoms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases |
| C0034372 |
BXGD002480 |
Quadriplegia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0034885 |
BXGD002490 |
Rectal Neoplasms |
Digestive System Diseases; Neoplasms |
| C0035067 |
BXGD002504 |
Renal Artery Stenosis |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Cardiovascular Diseases |
| C0035078 |
BXGD002505 |
Kidney Failure |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0035302 |
BXGD002527 |
Retinal Artery Occlusion |
Eye Diseases; Cardiovascular Diseases |
| C0035309 |
BXGD002530 |
Retinal Diseases |
Eye Diseases |
| C0035328 |
BXGD002537 |
Retinal Vein Occlusion |
Eye Diseases; Cardiovascular Diseases |
| C0035335 |
BXGD002540 |
Retinoblastoma |
Neoplasms; Eye Diseases |
| C0035344 |
BXGD002541 |
Retinopathy of Prematurity |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C0035439 |
BXGD002551 |
Rheumatic Heart Disease |
Infections; Cardiovascular Diseases |
| C0035528 |
BXGD002559 |
Riboflavin Deficiency |
Nutritional and Metabolic Diseases |
| C0036341 |
BXGD002600 |
Schizophrenia |
Mental Disorders |
| C0036346 |
BXGD002602 |
Schizophrenia, Childhood |
Mental Disorders |
| C0036421 |
BXGD002613 |
Systemic Scleroderma |
Skin and Connective Tissue Diseases |
| C0036572 |
BXGD002625 |
Seizures |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0036646 |
BXGD002627 |
Age-related cataract |
Eye Diseases |
| C0036690 |
BXGD002632 |
Septicemia |
Pathological Conditions, Signs and Symptoms; Infections |
| C0036857 |
BXGD002638 |
Severe intellectual disability |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0037054 |
BXGD002663 |
Sickle Cell Trait |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0037198 |
BXGD002670 |
Sinus Thrombosis, Intracranial |
Nervous System Diseases; Cardiovascular Diseases |
| C0037268 |
BXGD002675 |
Skin Abnormalities |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases |
| C0037274 |
BXGD002676 |
Dermatologic disorders |
Skin and Connective Tissue Diseases |
| C0037284 |
BXGD002679 |
Skin lesion |
Skin and Connective Tissue Diseases |
| C0037917 |
BXGD002711 |
Spina Bifida Cystica |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0037928 |
BXGD002713 |
Spinal Cord Diseases |
Nervous System Diseases |
| C0038013 |
BXGD002725 |
Ankylosing spondylitis |
Musculoskeletal Diseases |
| C0038219 |
BXGD002739 |
Status Dysraphicus |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0038279 |
BXGD002744 |
Sterility, Postpartum |
Female Urogenital Diseases and Pregnancy Complications |
| C0038356 |
BXGD002747 |
Stomach Neoplasms |
Digestive System Diseases; Neoplasms |
| C0038362 |
BXGD002749 |
Stomatitis |
Stomatognathic Diseases |
| C0038454 |
BXGD002760 |
Cerebrovascular accident |
Nervous System Diseases; Cardiovascular Diseases |
| C0038525 |
BXGD002768 |
Subarachnoid Hemorrhage |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases |
| C0039101 |
BXGD002790 |
synovial sarcoma |
Neoplasms |
| C0039240 |
BXGD002804 |
Supraventricular tachycardia |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0039263 |
BXGD002805 |
Takayasu Arteritis |
Skin and Connective Tissue Diseases; Cardiovascular Diseases |
| C0039483 |
BXGD002813 |
Giant Cell Arteritis |
Skin and Connective Tissue Diseases; Immune System Diseases; Nervous System Diseases; Cardiovascular Diseases |
| C0039494 |
BXGD002814 |
Temporomandibular Joint Disorders |
Musculoskeletal Diseases; Stomatognathic Diseases |
| C0039585 |
BXGD002821 |
Androgen-Insensitivity Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases |
| C0039685 |
BXGD002825 |
Tetralogy of Fallot |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C0040015 |
BXGD002833 |
Thrombasthenia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic 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 |
| C0040128 |
BXGD002844 |
Thyroid Diseases |
Endocrine System Diseases |
| C0040136 |
BXGD002845 |
Thyroid Neoplasm |
Neoplasms; Endocrine System Diseases |
| C0040156 |
BXGD002849 |
Thyrotoxicosis |
Endocrine System Diseases |
| C0040425 |
BXGD002863 |
Tonsillitis |
Infections; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases |
| C0041408 |
BXGD002923 |
Turner Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases; Cardiovascular Diseases |
| C0041696 |
BXGD002932 |
Unipolar Depression |
Mental Disorders |
| C0041755 |
BXGD002933 |
Adverse reaction to drug |
Chemically-Induced Disorders |
| C0041948 |
BXGD002939 |
Uremia |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0042341 |
BXGD002975 |
Varicocele |
Male Urogenital Diseases; Cardiovascular Diseases |
| C0042345 |
BXGD002977 |
Varicosity |
Cardiovascular Diseases |
| C0042373 |
BXGD002978 |
Vascular Diseases |
Cardiovascular Diseases |
| C0042487 |
BXGD002986 |
Venous Thrombosis |
Cardiovascular Diseases |
| C0042769 |
BXGD002999 |
Virus Diseases |
Infections |
| C0042847 |
BXGD003006 |
Vitamin B 12 Deficiency |
Nutritional and Metabolic Diseases |
| C0042900 |
BXGD003012 |
Vitiligo |
Skin and Connective Tissue Diseases |
| C0042974 |
BXGD003019 |
von Willebrand Disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0043144 |
BXGD003032 |
Wheezing |
Pathological Conditions, Signs and Symptoms |
| C0079102 |
BXGD003062 |
Cerebral Thrombosis |
Nervous System Diseases; Cardiovascular Diseases |
| C0079731 |
BXGD003087 |
B-Cell Lymphomas |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| 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 |
| C0079744 |
BXGD003090 |
Diffuse Large B-Cell Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0079745 |
BXGD003091 |
Lymphoma, Large-Cell, Follicular |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0079747 |
BXGD003093 |
Low Grade Lymphoma (neoplasm) |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0079748 |
BXGD003094 |
Precursor cell lymphoblastic lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0079757 |
BXGD003095 |
Diffuse Mixed-Cell Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0079758 |
BXGD003096 |
Lymphoma, Mixed-Cell, Follicular |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0079765 |
BXGD003097 |
Lymphoma, Small Cleaved-Cell, Follicular |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0079770 |
BXGD003098 |
Lymphoma, Small Noncleaved-Cell |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0079772 |
BXGD003099 |
T-Cell Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0080174 |
BXGD003106 |
Spina Bifida Occulta |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0080178 |
BXGD003107 |
Spina Bifida |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0080218 |
BXGD003109 |
Tethered Cord Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0085077 |
BXGD003117 |
Sweet Syndrome |
Skin and Connective Tissue Diseases |
| C0085083 |
BXGD003120 |
Ovarian Hyperstimulation Syndrome |
Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C0085096 |
BXGD003123 |
Peripheral Vascular Diseases |
Cardiovascular Diseases |
| C0085136 |
BXGD003131 |
Central Nervous System Neoplasms |
Neoplasms; Nervous System Diseases |
| C0085166 |
BXGD003136 |
Bacterial Vaginosis |
Female Urogenital Diseases and Pregnancy Complications; Infections |
| C0085183 |
BXGD003139 |
Neoplasms, Second Primary |
Neoplasms |
| C0085207 |
BXGD003140 |
Gestational Diabetes |
Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C0085215 |
BXGD003141 |
Ovarian Failure, Premature |
Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C0085278 |
BXGD003150 |
Antiphospholipid Syndrome |
Immune System Diseases |
| C0085281 |
BXGD003152 |
Addictive Behavior |
Behavior and Behavior Mechanisms |
| C0085409 |
BXGD003168 |
Polyendocrinopathies, Autoimmune |
Immune System Diseases; Endocrine System Diseases |
| C0085580 |
BXGD003191 |
Essential Hypertension |
Cardiovascular Diseases |
| C0085652 |
BXGD003224 |
Pyoderma Gangrenosum |
Skin and Connective Tissue Diseases |
| C0085669 |
BXGD003233 |
Acute leukemia |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0086132 |
BXGD003264 |
Depressive Symptoms |
Behavior and Behavior Mechanisms |
| C0086133 |
BXGD003265 |
Depressive Syndrome |
Mental Disorders |
| C0086445 |
BXGD003285 |
Idiopathic Membranous Glomerulonephritis |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases |
| C0086543 |
BXGD003294 |
Cataract |
Eye Diseases |
| C0086565 |
BXGD003295 |
Liver Dysfunction |
Digestive System Diseases |
| C0086664 |
BXGD003304 |
Myelocele |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0086873 |
BXGD003313 |
Pseudopelade |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases |
| C0086981 |
BXGD003317 |
Sicca Syndrome |
Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases; Stomatognathic Diseases |
| C0087169 |
BXGD003321 |
Withdrawal Symptoms |
Chemically-Induced Disorders; Mental Disorders |
| C0149521 |
BXGD003328 |
Pancreatitis, Chronic |
Digestive System Diseases |
| C0149721 |
BXGD003349 |
Left Ventricular Hypertrophy |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0149745 |
BXGD003356 |
Oral Ulcer |
Stomatognathic Diseases |
| C0149871 |
BXGD003375 |
Deep Vein Thrombosis |
Cardiovascular Diseases |
| C0149925 |
BXGD003387 |
Small cell carcinoma of lung |
Neoplasms; Respiratory Tract Diseases |
| C0149931 |
BXGD003388 |
Migraine Disorders |
Nervous System Diseases |
| C0150055 |
BXGD003401 |
Chronic pain |
Pathological Conditions, Signs and Symptoms |
| C0151281 |
BXGD003409 |
Genital ulcers |
|
| C0151313 |
BXGD003413 |
Sensory neuropathy |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0151449 |
BXGD003419 |
Primary Sjögren's syndrome |
Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases; Stomatognathic Diseases |
| C0151526 |
BXGD003432 |
Premature Birth |
Female Urogenital Diseases and Pregnancy Complications |
| C0151546 |
BXGD003437 |
Oral Cavity Carcinoma |
Digestive System Diseases; Neoplasms; Stomatognathic Diseases |
| C0151744 |
BXGD003469 |
Myocardial Ischemia |
Cardiovascular Diseases |
| C0151786 |
BXGD003475 |
Muscle Weakness |
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System 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 |
| C0152021 |
BXGD003520 |
Congenital heart disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C0152096 |
BXGD003538 |
Complete trisomy 18 syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C0152136 |
BXGD003548 |
Low Tension Glaucoma |
Eye Diseases |
| C0152234 |
BXGD003566 |
Iniencephaly |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0152426 |
BXGD003589 |
Craniorachischisis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0153381 |
BXGD003626 |
Malignant neoplasm of mouth |
Neoplasms; Stomatognathic Diseases |
| C0153452 |
BXGD003647 |
Malignant neoplasm of gallbladder |
Digestive System Diseases; Neoplasms |
| C0154409 |
BXGD003717 |
Recurrent major depressive episodes |
Mental Disorders |
| C0154575 |
BXGD003722 |
Rumination Disorders |
Mental Disorders |
| C0154723 |
BXGD003737 |
Migraine with Aura |
Nervous System Diseases |
| C0154830 |
BXGD003746 |
Proliferative diabetic retinopathy |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases |
| C0154841 |
BXGD003749 |
Central retinal vein occlusion |
Eye Diseases; Nervous System Diseases; Cardiovascular Diseases |
| C0155305 |
BXGD003785 |
Optic Neuropathy, Ischemic |
Eye Diseases; Nervous System Diseases; Cardiovascular Diseases |
| C0155626 |
BXGD003806 |
Acute myocardial infarction |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0155765 |
BXGD003819 |
Disease of capillaries |
Cardiovascular Diseases |
| C0155773 |
BXGD003820 |
Portal Vein Thrombosis |
Cardiovascular Diseases |
| C0156147 |
BXGD003838 |
Crohn's disease of large bowel |
Digestive System Diseases |
| C0158629 |
BXGD003895 |
Congenital anomaly of aortic arch |
Respiratory Tract Diseases; Cardiovascular Diseases |
| C0158646 |
BXGD003897 |
Cleft palate with cleft lip |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases |
| C0162311 |
BXGD003935 |
Androgenetic Alopecia |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases |
| C0162429 |
BXGD003942 |
Malnutrition |
Nutritional and Metabolic Diseases |
| C0162529 |
BXGD003948 |
Colitis, Ischemic |
Digestive System Diseases; Cardiovascular Diseases |
| C0162635 |
BXGD003964 |
Angelman Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0162739 |
BXGD003979 |
HELLP Syndrome |
Female Urogenital Diseases and Pregnancy Complications |
| C0162871 |
BXGD003996 |
Aortic Aneurysm, Abdominal |
Cardiovascular Diseases |
| C0202252 |
BXGD004089 |
VITAMIN B12 MEASUREMENT |
|
| C0206064 |
BXGD004150 |
Microvascular Angina |
Cardiovascular Diseases |
| C0206139 |
BXGD004159 |
Lichen Planus, Oral |
Skin and Connective Tissue Diseases; Stomatognathic Diseases |
| C0206368 |
BXGD004176 |
Exfoliation Syndrome |
Eye Diseases |
| C0206669 |
BXGD004229 |
Hepatocellular Adenoma |
Digestive System Diseases; Neoplasms |
| C0206677 |
BXGD004234 |
Adenomatous Polyps |
Neoplasms |
| C0206698 |
BXGD004248 |
Cholangiocarcinoma |
Neoplasms |
| C0206708 |
BXGD004256 |
Cervical Intraepithelial Neoplasia |
Neoplasms |
| C0220605 |
BXGD004294 |
Adult Non-Hodgkin Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0220612 |
BXGD004296 |
Childhood Non-Hodgkin Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0220615 |
BXGD004298 |
Adult Acute Myeloblastic Leukemia |
Neoplasms |
| C0220630 |
BXGD004302 |
Adult Liver Carcinoma |
Digestive System Diseases; Neoplasms |
| C0220641 |
BXGD004305 |
Lip and Oral Cavity Carcinoma |
Neoplasms; Stomatognathic Diseases |
| C0220668 |
BXGD004317 |
Congenital contractural arachnodactyly |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0220810 |
BXGD004346 |
Congenital defects |
|
| C0221065 |
BXGD004386 |
Subacute Combined Degeneration |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0221074 |
BXGD004388 |
Depression, Postpartum |
Female Urogenital Diseases and Pregnancy Complications; Mental Disorders |
| C0221165 |
BXGD004396 |
Diplegia |
|
| C0221166 |
BXGD004397 |
Paraparesis |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0221347 |
BXGD004442 |
Acrocyanosis |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases; Respiratory Tract Diseases; Cardiovascular Diseases |
| C0221505 |
BXGD004466 |
Lesion of brain |
|
| C0233514 |
BXGD004584 |
Abnormal behavior |
Behavior and Behavior Mechanisms |
| C0234985 |
BXGD004708 |
Mental deterioration |
Mental Disorders |
| C0235031 |
BXGD004714 |
Neurologic Symptoms |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0235522 |
BXGD004752 |
Disorder of vein |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0235782 |
BXGD004769 |
Gallbladder Carcinoma |
Digestive System Diseases; Neoplasms |
| C0235974 |
BXGD004796 |
Pancreatic carcinoma |
Digestive System Diseases; Neoplasms; Endocrine System Diseases |
| C0236734 |
BXGD004823 |
Caffeine related disorders |
|
| C0236788 |
BXGD004829 |
Bipolar II disorder |
Mental Disorders |
| C0236792 |
BXGD004830 |
Asperger Syndrome |
Mental Disorders |
| C0238457 |
BXGD004935 |
Thrombosis of renal vein |
Cardiovascular Diseases |
| C0238463 |
BXGD004938 |
Papillary thyroid carcinoma |
Neoplasms; Endocrine System Diseases |
| 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 |
| C0241950 |
BXGD005127 |
Intestinal infarction |
|
| C0242129 |
BXGD005136 |
Thrombotic stroke |
Nervous System Diseases; Cardiovascular Diseases |
| C0242231 |
BXGD005144 |
Coronary Stenosis |
Cardiovascular Diseases |
| C0242339 |
BXGD005150 |
Dyslipidemias |
Nutritional and Metabolic Diseases |
| C0242350 |
BXGD005154 |
Erectile dysfunction |
Male Urogenital Diseases; Mental Disorders |
| C0242379 |
BXGD005157 |
Malignant neoplasm of lung |
Neoplasms; Respiratory Tract Diseases |
| C0242647 |
BXGD005184 |
Mucosa-Associated Lymphoid Tissue Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0242666 |
BXGD005185 |
Protein S Deficiency |
Hemic and Lymphatic Diseases |
| C0243026 |
BXGD005210 |
Sepsis |
Pathological Conditions, Signs and Symptoms; Infections |
| C0262584 |
BXGD005256 |
Carcinoma, Small Cell |
Neoplasms |
| C0262586 |
BXGD005258 |
Osteopenia/osteoporosis |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C0263361 |
BXGD005292 |
Psoriasis vulgaris |
Skin and Connective Tissue Diseases |
| C0263477 |
BXGD005311 |
Female pattern alopecia (disorder) |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases |
| C0263725 |
BXGD005345 |
Hemophilic arthropathy |
Musculoskeletal Diseases |
| C0264408 |
BXGD005387 |
Childhood asthma |
Respiratory Tract Diseases; Immune System Diseases |
| C0264657 |
BXGD005409 |
Renal sclerosis with hypertension |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Cardiovascular Diseases |
| C0265706 |
BXGD005570 |
Gastroschisis |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0266453 |
BXGD005671 |
Exencephaly |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0266508 |
BXGD005684 |
Rachischisis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0267380 |
BXGD005743 |
Crohn's disease of the ileum |
Digestive System Diseases |
| C0268074 |
BXGD005810 |
Indian childhood cirrhosis |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Respiratory Tract Diseases |
| C0268138 |
BXGD005833 |
Xeroderma Pigmentosum, Complementation Group D |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases |
| C0268583 |
BXGD005997 |
Methylmalonic acidemia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0268611 |
BXGD006007 |
Arakawa syndrome 2 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0268615 |
BXGD006009 |
5,10-Methylenetetrahydrofolate reductase deficiency |
Nutritional and Metabolic Diseases |
| C0270612 |
BXGD006081 |
Leukoencephalopathy |
Nervous System Diseases |
| C0270639 |
BXGD006082 |
Lateral Sinus Thrombosis |
Nervous System Diseases; Cardiovascular Diseases |
| C0270736 |
BXGD006096 |
Essential Tremor |
Nervous System Diseases |
| C0271084 |
BXGD006159 |
Exudative age-related macular degeneration |
Eye Diseases |
| C0271680 |
BXGD006232 |
Diabetic Polyneuropathies |
Nervous System Diseases; Endocrine System Diseases |
| C0272322 |
BXGD006343 |
Severe hereditary factor VIII deficiency disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0272375 |
BXGD006359 |
Antithrombin III Deficiency |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0274861 |
BXGD006372 |
Arsenic Poisoning, Inorganic |
Nervous System Diseases; Chemically-Induced Disorders |
| C0274862 |
BXGD006373 |
Nervous System, Organic Arsenic Poisoning |
Nervous System Diseases; Chemically-Induced Disorders |
| C0276496 |
BXGD006426 |
Familial Alzheimer Disease (FAD) |
Nervous System Diseases; Mental Disorders |
| C0277005 |
BXGD006458 |
Opisthorchis viverrini Infection |
Infections |
| C0278480 |
BXGD006510 |
Stage III Colon Cancer |
Digestive System Diseases; Neoplasms |
| C0278484 |
BXGD006511 |
Malignant neoplasm of colon stage IV |
Digestive System Diseases; Neoplasms |
| C0278701 |
BXGD006566 |
Gastric Adenocarcinoma |
Digestive System Diseases; Neoplasms |
| C0278704 |
BXGD006567 |
Malignant Childhood Neoplasm |
Neoplasms |
| C0278721 |
BXGD006572 |
Adult Lymphoblastic Lymphoma |
|
| C0278877 |
BXGD006608 |
Adult Meningioma |
Neoplasms; Nervous System Diseases |
| C0278987 |
BXGD006620 |
Metastatic non-small cell lung cancer |
Neoplasms |
| C0278996 |
BXGD006621 |
Malignant Head and Neck Neoplasm |
Neoplasms |
| C0279000 |
BXGD006622 |
Liver and Intrahepatic Biliary Tract Carcinoma |
Digestive System Diseases; Neoplasms |
| C0279068 |
BXGD006624 |
Childhood Solid Neoplasm |
|
| C0279525 |
BXGD006627 |
Childhood Lymphoblastic Lymphoma |
|
| C0279593 |
BXGD006644 |
Adult B Acute Lymphoblastic Leukemia |
|
| C0279606 |
BXGD006647 |
Childhood Hepatocellular Carcinoma |
Digestive System Diseases; Neoplasms |
| C0279607 |
BXGD006648 |
Adult Hepatocellular Carcinoma |
Digestive System Diseases; Neoplasms |
| C0279626 |
BXGD006657 |
Squamous cell carcinoma of esophagus |
Digestive System Diseases; Neoplasms |
| C0279628 |
BXGD006659 |
Adenocarcinoma Of Esophagus |
Digestive System Diseases; Neoplasms |
| C0279680 |
BXGD006680 |
Transitional cell carcinoma of bladder |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0279702 |
BXGD006685 |
Conventional (Clear Cell) Renal Cell Carcinoma |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0280099 |
BXGD006712 |
Adult Solid Neoplasm |
|
| C0280100 |
BXGD006713 |
Solid Neoplasm |
Neoplasms |
| C0280803 |
BXGD006766 |
Primary central nervous system lymphoma |
Neoplasms; Immune System Diseases; Nervous System Diseases; Hemic and Lymphatic Diseases |
| C0282126 |
BXGD006796 |
Depression, Neurotic |
Mental Disorders |
| C0302142 |
BXGD006831 |
Deformity |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C0302592 |
BXGD006851 |
Cervix carcinoma |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications |
| C0311370 |
BXGD006882 |
Lupus anticoagulant disorder |
Pathological Conditions, Signs and Symptoms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0311375 |
BXGD006883 |
Arsenic Poisoning |
Nervous System Diseases; Chemically-Induced Disorders |
| C0314719 |
BXGD006890 |
Dryness of eye |
Eye Diseases |
| C0332853 |
BXGD006901 |
Anastomosis |
|
| C0333355 |
BXGD006950 |
Inflammatory disease of mucous membrane |
Digestive System Diseases; Stomatognathic Diseases |
| C0333516 |
BXGD006957 |
Tumor necrosis |
Pathological Conditions, Signs and Symptoms |
| C0333641 |
BXGD006961 |
Atrophic |
Pathological Conditions, Signs and Symptoms |
| C0333873 |
BXGD006971 |
Squamous intraepithelial lesion |
Pathological Conditions, Signs and Symptoms; Neoplasms; Female Urogenital Diseases and Pregnancy Complications |
| C0333983 |
BXGD006975 |
Hyperplastic Polyp |
Pathological Conditions, Signs and Symptoms |
| C0334294 |
BXGD007025 |
Multiple adenomatous polyps |
Neoplasms |
| C0338480 |
BXGD007186 |
Common Migraine |
Nervous System Diseases |
| C0338507 |
BXGD007195 |
Non-arteritic ischemic optic neuropathy |
Eye Diseases; Nervous System Diseases; Cardiovascular Diseases |
| C0338573 |
BXGD007199 |
Cerebral venous sinus thrombosis |
Nervous System Diseases; Cardiovascular Diseases |
| C0338656 |
BXGD007211 |
Impaired cognition |
Mental Disorders |
| C0338831 |
BXGD007216 |
Manic |
Mental Disorders |
| C0338908 |
BXGD007218 |
Mixed anxiety and depressive disorder |
Mental Disorders |
| C0339143 |
BXGD007226 |
Thyroid associated opthalmopathies |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Immune System Diseases; Endocrine System Diseases |
| C0339467 |
BXGD007248 |
Proliferative retinopathy |
Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases |
| C0339505 |
BXGD007255 |
Venous retinal branch occlusion |
Eye Diseases; Cardiovascular Diseases |
| C0339573 |
BXGD007271 |
Glaucoma, Primary Open Angle |
Eye Diseases |
| C0340293 |
BXGD007318 |
Anterior myocardial infarction |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0340324 |
BXGD007321 |
Silent myocardial infarction |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0340968 |
BXGD007377 |
Deficiency of pyruvate kinase |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases |
| C0341869 |
BXGD007427 |
Subfertility, Female |
Female Urogenital Diseases and Pregnancy Complications |
| C0342257 |
BXGD007447 |
Complications of Diabetes Mellitus |
Endocrine System Diseases |
| C0342637 |
BXGD007517 |
Hypocalciuric hypercalcemia, familial, type 1 |
Nutritional and Metabolic Diseases |
| C0342882 |
BXGD007573 |
Familial hypercholesterolemia - heterozygous |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0343525 |
BXGD007631 |
Lemierre Syndrome |
Infections; Stomatognathic Diseases; Otorhinolaryngologic Diseases; Cardiovascular Diseases |
| C0343641 |
BXGD007636 |
Human papilloma virus infection |
Infections |
| C0344315 |
BXGD007666 |
Depressed mood |
Behavior and Behavior Mechanisms |
| C0344479 |
BXGD007677 |
Spinal Cord Myelodysplasia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0344622 |
BXGD007697 |
Double inlet left ventricle |
|
| C0344724 |
BXGD007701 |
Ostium secundum atrial septal defect |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C0345904 |
BXGD007745 |
Malignant neoplasm of liver |
Digestive System Diseases; Neoplasms |
| C0345905 |
BXGD007746 |
Intrahepatic Cholangiocarcinoma |
Neoplasms |
| C0346153 |
BXGD007781 |
Breast Cancer, Familial |
Neoplasms; Skin and Connective Tissue Diseases |
| C0346647 |
BXGD007832 |
Malignant neoplasm of pancreas |
Digestive System Diseases; Neoplasms; Endocrine System Diseases |
| C0349204 |
BXGD007892 |
Nonorganic psychosis |
Mental Disorders |
| C0349458 |
BXGD007906 |
Cervical intraepithelial neoplasia grade 1 |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications |
| C0349459 |
BXGD007907 |
Cervical intraepithelial neoplasia grade 2 |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications |
| C0374997 |
BXGD007967 |
Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site |
|
| C0376286 |
BXGD007984 |
Avitaminosis |
Nutritional and Metabolic Diseases |
| C0376338 |
BXGD007990 |
Diagnosis, Psychiatric |
Mental Disorders |
| C0376358 |
BXGD007992 |
Malignant neoplasm of prostate |
Neoplasms; Male Urogenital Diseases |
| C0376545 |
BXGD008002 |
Hematologic Neoplasms |
Neoplasms; Hemic and Lymphatic Diseases |
| C0393706 |
BXGD008126 |
Early infantile epileptic encephalopathy with suppression bursts |
Nervous System Diseases |
| C0393992 |
BXGD008162 |
Multicystic Encephalomalacia |
Nervous System Diseases |
| C0398621 |
BXGD008201 |
Hypoplasminogenemia |
Hemic and Lymphatic Diseases |
| C0398623 |
BXGD008202 |
Thrombophilia |
Hemic and Lymphatic Diseases |
| C0398625 |
BXGD008203 |
Protein C Deficiency |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0400966 |
BXGD008266 |
Non-alcoholic Fatty Liver Disease |
Digestive System Diseases |
| C0403592 |
BXGD008297 |
Chronic rejection of renal transplant |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0403823 |
BXGD008315 |
Asthenozoospermia |
Male Urogenital Diseases |
| C0406317 |
BXGD008334 |
Chronic small plaque psoriasis |
Skin and Connective Tissue Diseases |
| C0406537 |
BXGD008348 |
Morbilliform Drug Reaction |
Skin and Connective Tissue Diseases; Immune System Diseases; Chemically-Induced Disorders |
| C0409974 |
BXGD008401 |
Lupus Erythematosus |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases; Immune System Diseases |
| C0409980 |
BXGD008403 |
Primary antiphospholipid syndrome |
Immune System Diseases |
| C0424295 |
BXGD008524 |
Hyperactive behavior |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0424605 |
BXGD008535 |
Developmental delay (disorder) |
Mental Disorders |
| C0427418 |
BXGD008614 |
Folic acid measurement, RBC |
|
| C0427460 |
BXGD008616 |
Red cell distribution width determination |
|
| C0428883 |
BXGD008639 |
Diastolic blood pressure |
|
| C0428886 |
BXGD008640 |
Mean blood pressure |
|
| C0432416 |
BXGD008788 |
Down Syndrome, Partial Trisomy 21 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0432417 |
BXGD008789 |
Trisomy 21, Meiotic Nondisjunction |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| 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 |
| C0476089 |
BXGD008977 |
Endometrial Carcinoma |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications |
| C0494165 |
BXGD009022 |
Secondary malignant neoplasm of liver |
Digestive System Diseases; Neoplasms |
| C0494463 |
BXGD009029 |
Alzheimer Disease, Late Onset |
Nervous System Diseases; Mental Disorders |
| C0497327 |
BXGD009061 |
Dementia |
Nervous System Diseases; Mental Disorders |
| C0520679 |
BXGD009101 |
Sleep Apnea, Obstructive |
Respiratory Tract Diseases; Nervous System Diseases |
| C0520966 |
BXGD009128 |
Abnormal coordination |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0521170 |
BXGD009131 |
Osteoporotic Fractures |
Wounds and Injuries |
| C0521585 |
BXGD009145 |
Gastrointestinal mucositis |
Digestive System Diseases; Stomatognathic Diseases |
| C0522254 |
BXGD009199 |
Analgesic Overuse Headache |
Nervous System Diseases |
| C0523631 |
BXGD009213 |
Folic acid measurement |
|
| C0524528 |
BXGD009229 |
Pervasive Development Disorder |
Mental Disorders |
| C0524620 |
BXGD009236 |
Metabolic Syndrome X |
Nutritional and Metabolic Diseases |
| C0524702 |
BXGD009242 |
Pulmonary Thromboembolisms |
Respiratory Tract Diseases; Cardiovascular Diseases |
| C0524851 |
BXGD009246 |
Neurodegenerative Disorders |
Nervous System Diseases |
| C0524910 |
BXGD009248 |
Hepatitis C, Chronic |
Digestive System Diseases; Infections |
| C0524948 |
BXGD009251 |
Maxillofacial Abnormalities |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases |
| C0525045 |
BXGD009255 |
Mood Disorders |
Mental Disorders |
| C0543982 |
BXGD009304 |
Glaucoma, primary |
Eye Diseases |
| C0546126 |
BXGD009328 |
Acute Confusional Senile Dementia |
Nervous System Diseases; Mental Disorders |
| C0546837 |
BXGD009343 |
Malignant neoplasm of esophagus |
Digestive System Diseases; Neoplasms |
| C0549410 |
BXGD009378 |
Palmar-plantar erythrodysesthesia syndrome |
Skin and Connective Tissue Diseases; Chemically-Induced Disorders |
| C0549473 |
BXGD009384 |
Thyroid carcinoma |
Neoplasms; Endocrine System Diseases |
| C0553694 |
BXGD009409 |
Oropharyngeal disorders |
Digestive System Diseases; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases |
| C0553723 |
BXGD009416 |
Squamous cell carcinoma of skin |
Neoplasms; Skin and Connective Tissue Diseases |
| C0555198 |
BXGD009432 |
Malignant Glioma |
Neoplasms |
| C0557874 |
BXGD009444 |
Global developmental delay |
|
| C0559031 |
BXGD009464 |
Functional Gastrointestinal Disorders |
Digestive System Diseases |
| C0565599 |
BXGD009488 |
Maternal hypertension |
Female Urogenital Diseases and Pregnancy Complications; Cardiovascular Diseases |
| C0575081 |
BXGD009512 |
Gait abnormality |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0577631 |
BXGD009535 |
Carotid Atherosclerosis |
Nervous System Diseases; Cardiovascular Diseases |
| C0584960 |
BXGD009579 |
Factor V Leiden mutation |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0584984 |
BXGD009581 |
Heterozygous Factor V Leiden mutation |
|
| C0585442 |
BXGD009593 |
Osteosarcoma of bone |
Neoplasms |
| C0586323 |
BXGD009603 |
Alcohol Withdrawal Seizures |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Chemically-Induced Disorders |
| C0586354 |
BXGD009604 |
Esophageal dysplasia |
Digestive System Diseases; Neoplasms |
| C0588008 |
BXGD009620 |
Severe depression |
Mental Disorders |
| 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 |
| 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 |
| C0677659 |
BXGD009724 |
Gastro-esophageal reflux disease with esophagitis |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C0677660 |
BXGD009725 |
Emotional problems |
Mental Disorders |
| C0677949 |
BXGD009740 |
Stage III Colorectal Cancer |
Digestive System Diseases; Neoplasms |
| C0678202 |
BXGD009747 |
Regional enteritis |
Digestive System Diseases |
| C0678222 |
BXGD009749 |
Breast Carcinoma |
Neoplasms; Skin and Connective Tissue Diseases |
| C0684249 |
BXGD009790 |
Carcinoma of lung |
Neoplasms; Respiratory Tract Diseases |
| C0684275 |
BXGD009792 |
Hemophilia, NOS |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0685889 |
BXGD009823 |
Splenic Hypoplasia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases |
| C0685938 |
BXGD009829 |
Malignant neoplasm of gastrointestinal tract |
Digestive System Diseases; Neoplasms |
| C0686619 |
BXGD009835 |
Secondary malignant neoplasm of lymph node |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0687132 |
BXGD009839 |
heavy drinking |
|
| 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 |
| C0699893 |
BXGD009871 |
Skin carcinoma |
Neoplasms; Skin and Connective Tissue Diseases |
| C0700095 |
BXGD009875 |
Central neuroblastoma |
Neoplasms; Nervous System Diseases |
| C0702169 |
BXGD009914 |
Acrania |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0729353 |
BXGD009924 |
Subfertility |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0740394 |
BXGD009989 |
Hyperuricemia |
Pathological Conditions, Signs and Symptoms |
| C0740447 |
BXGD009998 |
Diabetic peripheral neuropathy |
Nervous System Diseases; Endocrine System Diseases |
| C0741923 |
BXGD010045 |
cardiac event |
|
| C0742343 |
BXGD010061 |
Acute Chest Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Hemic and Lymphatic Diseases |
| C0744669 |
BXGD010104 |
Complex congenital heart disease |
|
| C0745103 |
BXGD010114 |
Hyperlipoproteinemia Type IIa |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0745744 |
BXGD010133 |
End Stage Liver Disease |
Digestive System Diseases |
| C0746731 |
BXGD010148 |
Acute myocardial ischemia |
Cardiovascular Diseases |
| C0746883 |
BXGD010153 |
Febrile Neutropenia |
Hemic and Lymphatic Diseases |
| C0747845 |
BXGD010184 |
early pregnancy |
|
| C0750145 |
BXGD010227 |
Occlusive vascular disease |
|
| C0750151 |
BXGD010228 |
Vaso-Occlusive Crisis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0750900 |
BXGD010241 |
Alzheimer's Disease, Focal Onset |
Nervous System Diseases; Mental Disorders |
| C0750901 |
BXGD010242 |
Alzheimer Disease, Early Onset |
Nervous System Diseases; Mental Disorders |
| C0750927 |
BXGD010254 |
Apraxia, Developmental Verbal |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms |
| C0750974 |
BXGD010270 |
Brain Tumor, Primary |
Neoplasms; Nervous System Diseases |
| C0751007 |
BXGD010287 |
Intracranial Atherosclerosis |
Nervous System Diseases; Cardiovascular Diseases |
| C0751081 |
BXGD010315 |
Trisomy 21, Mitotic Nondisjunction |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous 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 |
| C0751295 |
BXGD010383 |
Memory Loss |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms |
| C0751316 |
BXGD010387 |
Acquired Meningomyelocele |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0751500 |
BXGD010475 |
Petrous Sinus Thrombophlebitis |
Nervous System Diseases; Cardiovascular Diseases |
| C0751501 |
BXGD010476 |
Intracranial Sinus Thrombophlebitis |
Nervous System Diseases; Cardiovascular Diseases |
| C0751502 |
BXGD010477 |
Petrous Sinus Thrombosis |
Nervous System Diseases; Cardiovascular Diseases |
| C0751606 |
BXGD010523 |
Adult Acute Lymphocytic Leukemia |
|
| C0751688 |
BXGD010551 |
Malignant Squamous Cell Neoplasm |
Neoplasms |
| C0751711 |
BXGD010563 |
Anterior Ischemic Optic Neuropathy |
Eye Diseases; Nervous System Diseases; Cardiovascular Diseases |
| C0751851 |
BXGD010610 |
Arsenic Encephalopathy |
Nervous System Diseases; Chemically-Induced Disorders |
| C0751852 |
BXGD010611 |
Arsenic Induced Polyneuropathy |
Nervous System Diseases; Chemically-Induced Disorders |
| C0751955 |
BXGD010652 |
Brain Infarction |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases |
| C0751956 |
BXGD010653 |
Acute Cerebrovascular Accidents |
Nervous System Diseases; Cardiovascular Diseases |
| C0751967 |
BXGD010657 |
Multiple Sclerosis, Relapsing-Remitting |
Immune System Diseases; Nervous System Diseases |
| C0752121 |
BXGD010669 |
Spinocerebellar Ataxia Type 2 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0795687 |
BXGD010726 |
Cerebral arterial thrombosis |
Nervous System Diseases; Cardiovascular Diseases |
| C0795690 |
BXGD010728 |
Congenital omphalocele |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C0810032 |
BXGD010843 |
Pancreatic disorders (not diabetes) |
Digestive System Diseases |
| C0810364 |
BXGD010846 |
Cleft Lip with or without Cleft Palate |
|
| C0848558 |
BXGD010882 |
Hypospadias |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0848676 |
BXGD010883 |
Subfertility, Male |
Male Urogenital Diseases |
| C0850666 |
BXGD010901 |
Infection caused by Helicobacter pylori |
Infections |
| C0851140 |
BXGD010916 |
Carcinoma in situ of uterine cervix |
Neoplasms |
| C0852036 |
BXGD010934 |
Pregnancy associated hypertension |
Female Urogenital Diseases and Pregnancy Complications; Cardiovascular Diseases |
| C0852077 |
BXGD010935 |
Blood Coagulation Disorders, Inherited |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0852711 |
BXGD010951 |
Sickle Cell Dactylitis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Chemically-Induced Disorders; Hemic and Lymphatic Diseases |
| C0852733 |
BXGD010952 |
Completed Suicide |
|
| C0852949 |
BXGD010957 |
Arteriopathic disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0853193 |
BXGD010968 |
Bipolar I disorder |
Mental Disorders |
| C0856053 |
BXGD011091 |
Leukemia secondary |
|
| C0856169 |
BXGD011096 |
Endothelial dysfunction |
|
| C0856761 |
BXGD011115 |
Budd-Chiari Syndrome |
Digestive System Diseases; Cardiovascular Diseases |
| C0856825 |
BXGD011118 |
Acute GVH disease |
Immune System Diseases |
| C0856862 |
BXGD011121 |
Posterior cerebral artery occlusion |
|
| C0857175 |
BXGD011140 |
Postinfarction |
|
| C0860207 |
BXGD011220 |
Drug-Induced Liver Disease |
Digestive System Diseases; Chemically-Induced Disorders |
| C0861461 |
BXGD011248 |
Stage IV Colon Carcinoma |
|
| C0868908 |
BXGD011302 |
Pancolitis |
Digestive System Diseases |
| C0871189 |
BXGD011312 |
Psychotic symptom |
|
| C0871470 |
BXGD011316 |
Systolic Pressure |
|
| C0872084 |
BXGD011319 |
Sarcopenia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0917730 |
BXGD011406 |
Female sterility |
Female Urogenital Diseases and Pregnancy Complications |
| C0917731 |
BXGD011407 |
Male sterility |
Male Urogenital Diseases |
| C0917796 |
BXGD011408 |
Optic Atrophy, Hereditary, Leber |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Nervous System Diseases |
| 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 |
| C0920028 |
BXGD011454 |
Leukaemia recurrent |
Neoplasms |
| C0920269 |
BXGD011462 |
Microsatellite Instability |
Pathological Conditions, Signs and Symptoms |
| C0936215 |
BXGD011476 |
Vitamin B 6 Deficiency |
Nutritional and Metabolic Diseases |
| C0948008 |
BXGD011499 |
Ischemic stroke |
Nervous System Diseases; Cardiovascular Diseases |
| C0948089 |
BXGD011504 |
Acute Coronary Syndrome |
Cardiovascular Diseases |
| C0948163 |
BXGD011511 |
Leukoaraiosis |
Pathological Conditions, Signs and Symptoms |
| C0948480 |
BXGD011540 |
Coronary Restenosis |
Cardiovascular Diseases |
| C0949059 |
BXGD011568 |
Polyp of large intestine |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Neoplasms |
| C0949272 |
BXGD011573 |
IIeocolitis |
Digestive System Diseases |
| C1096293 |
BXGD011616 |
Macroangiopathy |
|
| C1096458 |
BXGD011622 |
Vascular occlusion |
Cardiovascular Diseases |
| C1135868 |
BXGD011700 |
Gestational Trophoblastic Neoplasms |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications |
| C1140680 |
BXGD011718 |
Malignant neoplasm of ovary |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C1148477 |
BXGD011765 |
Deafness, Sudden |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases |
| C1167791 |
BXGD011776 |
Skin toxicity |
|
| C1168401 |
BXGD011792 |
Squamous cell carcinoma of the head and neck |
Neoplasms |
| C1257931 |
BXGD011815 |
Mammary Neoplasms, Human |
Neoplasms; Skin and Connective Tissue Diseases |
| C1260403 |
BXGD011832 |
prothrombin gene mutation |
Hemic and Lymphatic Diseases |
| C1261473 |
BXGD011855 |
Sarcoma |
Neoplasms |
| C1261502 |
BXGD011856 |
Finding of Mean Corpuscular Hemoglobin |
|
| C1262760 |
BXGD011886 |
Hepatitis, Drug-Induced |
Digestive System Diseases; Chemically-Induced Disorders |
| C1263846 |
BXGD011897 |
Attention deficit hyperactivity disorder |
Mental Disorders |
| C1269683 |
BXGD012001 |
Major Depressive Disorder |
Mental Disorders |
| C1269955 |
BXGD012005 |
Tumor Cell Invasion |
|
| C1270972 |
BXGD012006 |
Mild cognitive disorder |
Mental Disorders |
| C1273976 |
BXGD012020 |
First myocardial infarction |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C1275122 |
BXGD012060 |
Familial multiple trichoepitheliomata |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Skin and Connective Tissue Diseases |
| C1290884 |
BXGD012198 |
Inflammatory disorder |
Pathological Conditions, Signs and Symptoms |
| C1292769 |
BXGD012230 |
Precursor B-cell lymphoblastic leukemia |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C1298680 |
BXGD012247 |
Occlusive stroke |
Nervous System Diseases; Cardiovascular Diseases |
| C1299567 |
BXGD012260 |
Neonatal stroke |
Nervous System Diseases; Cardiovascular Diseases |
| C1301700 |
BXGD012296 |
Cardiovascular morbidity |
|
| C1302401 |
BXGD012303 |
Adenoma of large intestine |
Digestive System Diseases; Neoplasms |
| C1302773 |
BXGD012312 |
Low Grade Squamous Intraepithelial Neoplasia |
Pathological Conditions, Signs and Symptoms; Neoplasms; Female Urogenital Diseases and Pregnancy Complications |
| C1304746 |
BXGD012343 |
RDW - Red blood cell distribution width result |
|
| C1305849 |
BXGD012347 |
Diastolic blood pressure measurement |
|
| C1306459 |
BXGD012361 |
Primary malignant neoplasm |
Neoplasms |
| C1306460 |
BXGD012362 |
Primary malignant neoplasm of lung |
Neoplasms; Respiratory Tract Diseases |
| C1306620 |
BXGD012371 |
Systolic blood pressure measurement |
|
| C1306759 |
BXGD012374 |
Eosinophilic disorder |
Hemic and Lymphatic Diseases |
| C1306889 |
BXGD012380 |
Peripheral arterial occlusive disease |
Cardiovascular Diseases |
| C1319315 |
BXGD012415 |
Adenocarcinoma of large intestine |
Digestive System Diseases; Neoplasms |
| 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 |
| C1332922 |
BXGD012556 |
Cervical Squamous Intraepithelial Neoplasia |
Pathological Conditions, Signs and Symptoms; Neoplasms; Female Urogenital Diseases and Pregnancy Complications |
| C1332977 |
BXGD012569 |
Childhood Leukemia |
Neoplasms |
| C1332979 |
BXGD012571 |
Childhood Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C1332986 |
BXGD012574 |
Childhood Osteosarcoma |
Neoplasms |
| C1333015 |
BXGD012581 |
Childhood Kidney Wilms Tumor |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C1333419 |
BXGD012624 |
Liver and Intrahepatic Bile Duct Epithelial Neoplasm |
|
| C1333762 |
BXGD012639 |
Gastric Cardia Adenocarcinoma |
|
| C1333976 |
BXGD012662 |
Liver and Intrahepatic Bile Duct Neoplasm |
Digestive System Diseases |
| C1333990 |
BXGD012670 |
Hereditary Nonpolyposis Colorectal Cancer |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Nutritional and Metabolic Diseases |
| C1334177 |
BXGD012684 |
Infiltrating Cervical Carcinoma |
|
| C1336076 |
BXGD012828 |
Sporadic Breast Carcinoma |
Neoplasms; Skin and Connective Tissue Diseases |
| C1337013 |
BXGD012876 |
Differentiated Thyroid Gland Carcinoma |
|
| C1384666 |
BXGD012948 |
hearing impairment |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases |
| C1392786 |
BXGD012978 |
Cognitive changes |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C1402315 |
BXGD013017 |
Vascular lesions |
|
| C1442965 |
BXGD013064 |
Avascular necrosis of the capital femoral epiphysis |
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases |
| C1443924 |
BXGD013074 |
Severe diarrhea |
Pathological Conditions, Signs and Symptoms |
| C1456873 |
BXGD013129 |
alpha^+^ Thalassemia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C1458155 |
BXGD013136 |
Mammary Neoplasms |
Neoplasms; Skin and Connective Tissue Diseases |
| C1510431 |
BXGD013162 |
Superficial Thrombophlebitis |
Cardiovascular Diseases |
| C1510471 |
BXGD013169 |
Vitamin Deficiency |
Nutritional and Metabolic Diseases |
| C1510586 |
BXGD013176 |
Autism Spectrum Disorders |
Mental Disorders |
| C1516490 |
BXGD013214 |
Cholangiolocellular Carcinoma |
Neoplasms |
| C1519689 |
BXGD013245 |
Tumor Promotion |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C1527304 |
BXGD013266 |
Allergic Reaction |
Immune System Diseases |
| C1527411 |
BXGD013292 |
Thrombosis of retinal vein |
Eye Diseases; Cardiovascular Diseases |
| C1531624 |
BXGD013300 |
Cardioembolic stroke |
|
| C1536220 |
BXGD013341 |
ST segment elevation myocardial infarction |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C1561643 |
BXGD013363 |
Chronic Kidney Diseases |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C1563715 |
BXGD013389 |
Andersen Syndrome |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C1565321 |
BXGD013400 |
Cholera Infantum |
Digestive System Diseases |
| C1565489 |
BXGD013401 |
Renal Insufficiency |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C1565662 |
BXGD013402 |
Acute Kidney Insufficiency |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C1567742 |
BXGD013415 |
Alport Syndrome, X-Linked |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases; Male Urogenital Diseases |
| C1568868 |
BXGD013423 |
Oral Mucositis |
Stomatognathic Diseases |
| C1610621 |
BXGD013451 |
Factor II mutation |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C1611743 |
BXGD013456 |
Familial (FPAH) |
|
| C1621958 |
BXGD013468 |
Glioblastoma Multiforme |
Neoplasms |
| C1623038 |
BXGD013475 |
Cirrhosis |
Pathological Conditions, Signs and Symptoms |
| C1691215 |
BXGD013491 |
Penile hypospadias |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C1704272 |
BXGD013537 |
Benign Prostatic Hyperplasia |
Male Urogenital Diseases |
| C1704321 |
BXGD013544 |
Nephrotic Syndrome, Minimal Change |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C1704436 |
BXGD013564 |
Peripheral Arterial Diseases |
Cardiovascular Diseases |
| C1705254 |
BXGD013568 |
Neonatal Deformity |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C1708349 |
BXGD013597 |
Hereditary Diffuse Gastric Cancer |
Digestive System Diseases; Neoplasms |
| C1721098 |
BXGD013705 |
Replication Error Phenotype |
Pathological Conditions, Signs and Symptoms |
| C1737329 |
BXGD013728 |
Dysmorphism |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C1739111 |
BXGD013731 |
Fetus affected by placental transfer of anticonvulsant |
|
| C1762616 |
BXGD013753 |
Meningioma, benign, no ICD-O subtype |
Neoplasms; Nervous System Diseases |
| C1827377 |
BXGD013770 |
Slow acetylator due to N-acetyltransferase enzyme variant |
|
| C1827820 |
BXGD013778 |
Fast acetylator due to N-acetyltransferase enzyme variant |
|
| C1837218 |
BXGD014207 |
Cleft palate, isolated |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases |
| C1837352 |
BXGD014223 |
Childhood onset |
|
| C1840311 |
BXGD014445 |
Laryngeal cleft |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C1842704 |
BXGD014534 |
GAUCHER DISEASE, PERINATAL LETHAL |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C1842981 |
BXGD014547 |
NEUROTICISM |
Behavior and Behavior Mechanisms |
| C1843013 |
BXGD014549 |
Alzheimer disease, familial, type 3 |
Nervous System Diseases; Mental Disorders |
| C1845026 |
BXGD014700 |
Neural tube defects X-linked |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C1845027 |
BXGD014701 |
Spina Bifida, X-Linked |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C1847540 |
BXGD014874 |
Azoospermia, Nonobstructive |
Male Urogenital Diseases |
| C1847835 |
BXGD014892 |
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding) |
Skin and Connective Tissue Diseases |
| C1848533 |
BXGD014936 |
Ataxia with vitamin E deficiency |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C1850406 |
BXGD015140 |
NAVAJO NEUROHEPATOPATHY |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C1850900 |
BXGD015186 |
Familial primary gastric lymphoma |
Digestive System Diseases; Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C1852242 |
BXGD015266 |
Nonarteritic anterior ischemic optic neuropathy (NAION) |
|
| C1853238 |
BXGD015320 |
Conotruncal defect |
|
| C1855119 |
BXGD015463 |
Methylmalonic aciduria |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C1855128 |
BXGD015465 |
Methylcobalamin Deficiency, CblG Type |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C1856058 |
BXGD015568 |
HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATE REDUCTASE ACTIVITY |
|
| C1856059 |
BXGD015569 |
Mthfr Deficiency, Thermolabile Type |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Nervous System Diseases |
| C1856061 |
BXGD015570 |
Methylenetetrahydrofolate reductase deficiency |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders |
| C1856689 |
BXGD015630 |
FRIEDREICH ATAXIA 1 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C1858991 |
BXGD015841 |
Childhood Ataxia with Central Nervous System Hypomyelinization |
Nervous System Diseases |
| C1859726 |
BXGD015926 |
ARTERIAL TORTUOSITY SYNDROME |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases |
| C1861172 |
BXGD016016 |
Venous Thromboembolism |
Cardiovascular Diseases |
| C1861305 |
BXGD016027 |
TARSAL-CARPAL COALITION SYNDROME |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C1861453 |
BXGD016049 |
Pseudohyperkalemia Cardiff |
Nutritional and Metabolic Diseases |
| C1861537 |
BXGD016058 |
OROFACIAL CLEFT 1 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases |
| C1862389 |
BXGD016126 |
ATRIAL SEPTAL DEFECT 1 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C1862941 |
BXGD016145 |
Amyotrophic Lateral Sclerosis, Sporadic |
Nutritional and Metabolic Diseases; Nervous System Diseases |
| C1866558 |
BXGD016409 |
Neural tube defect, folate-sensitive |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C1866559 |
BXGD016410 |
Spina Bifida, Folate-Sensitive |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C1866986 |
BXGD016430 |
Social and occupational deterioration |
Mental Disorders |
| C1867743 |
BXGD016470 |
Premature coronary artery atherosclerosis |
Cardiovascular Diseases |
| C1956130 |
BXGD016619 |
Lymphoma, Follicular, Grade 1 |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C1956131 |
BXGD016620 |
Lymphoma, Follicular, Grade 3 |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C1956132 |
BXGD016621 |
Lymphoma, Follicular, Grade 2 |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C1956346 |
BXGD016627 |
Coronary Artery Disease |
Cardiovascular Diseases |
| C1960883 |
BXGD016670 |
Spina bifida aperta of cervical spine |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C1961102 |
BXGD016673 |
Precursor Cell Lymphoblastic Leukemia Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C1963943 |
BXGD016706 |
Atherothrombosis |
|
| C2145472 |
BXGD016931 |
Urothelial Carcinoma |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C2217040 |
BXGD016954 |
malignant neoplasm of large intestine stage IV |
|
| C2239176 |
BXGD016965 |
Liver carcinoma |
Digestive System Diseases; Neoplasms |
| C2242817 |
BXGD017005 |
Homocysteine measurement |
|
| C2314994 |
BXGD017020 |
Infarction of spinal cord |
Nervous System Diseases; Cardiovascular Diseases; Wounds and Injuries |
| C2316810 |
BXGD017030 |
Chronic kidney disease stage 5 |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C2584409 |
BXGD017126 |
Prothrombin G20210A mutation |
Hemic and Lymphatic Diseases |
| C2584620 |
BXGD017129 |
Thrombophilia, hereditary |
Hemic and Lymphatic Diseases |
| C2585317 |
BXGD017135 |
Acquired thrombophilia |
Hemic and Lymphatic Diseases |
| C2607914 |
BXGD017148 |
Allergic rhinitis (disorder) |
Respiratory Tract Diseases; Immune System Diseases; Otorhinolaryngologic Diseases |
| C2609259 |
BXGD017173 |
Symphysis Pubis Dysfunction |
Pathological Conditions, Signs and Symptoms |
| C2609414 |
BXGD017182 |
Acute kidney injury |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C2711227 |
BXGD017478 |
Steatohepatitis |
Digestive System Diseases |
| C2717961 |
BXGD017519 |
Thrombotic Microangiopathies |
Hemic and Lymphatic Diseases |
| C2721734 |
BXGD017549 |
Methylenetetrahydrofolate reductase polymorphism |
Hemic and Lymphatic Diseases |
| C2733158 |
BXGD017562 |
Cerebral Small Vessel Diseases |
Nervous System Diseases; Cardiovascular Diseases |
| C2745948 |
BXGD017569 |
Hyalinosis, Systemic |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases |
| C2826025 |
BXGD017783 |
Mixed phenotype acute leukemia |
|
| C2931384 |
BXGD018014 |
Moyamoya disease 1 |
Nervous System Diseases; Cardiovascular Diseases |
| C2931822 |
BXGD018068 |
Nasopharyngeal carcinoma |
Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic 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 |
| C2937365 |
BXGD018161 |
Recurrent aphthous ulcer |
Stomatognathic Diseases |
| C2939419 |
BXGD018178 |
Secondary Neoplasm |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C2939465 |
BXGD018182 |
Deficiency of glucose-6-phosphate dehydrogenase |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases |
| C2945695 |
BXGD018187 |
Limb ischemia |
|
| C2981150 |
BXGD018211 |
Uranostaphyloschisis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases |
| C3146250 |
BXGD018259 |
Stage III Colorectal Cancer AJCC v7 |
|
| C3146254 |
BXGD018263 |
Stage III Colon Cancer AJCC v7 |
|
| C3160718 |
BXGD018468 |
PARKINSON DISEASE, LATE-ONSET |
|
| C3160733 |
BXGD018471 |
THROMBOPHILIA DUE TO THROMBIN DEFECT |
|
| C3178801 |
BXGD018538 |
Stroke, Lacunar |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases |
| C3241937 |
BXGD018578 |
Nonalcoholic Steatohepatitis |
Digestive System Diseases |
| C3266262 |
BXGD018600 |
Multiple Chronic Conditions |
Pathological Conditions, Signs and Symptoms |
| C3272265 |
BXGD018618 |
Three Vessel Coronary Disease |
|
| 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 |
| C3489532 |
BXGD018934 |
Cone-Rod Dystrophy 2 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C3495426 |
BXGD018983 |
Homocysteinemia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C3495549 |
BXGD018991 |
Patent ductus arteriosus - persisting type |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Cardiovascular Diseases |
| C3495559 |
BXGD018994 |
Juvenile arthritis |
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases |
| C3495676 |
BXGD019000 |
Anorectal Malformations |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases |
| C3495917 |
BXGD019012 |
Advanced breast cancer |
|
| C3496337 |
BXGD019020 |
Idiopathic Nephrotic Syndrome |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C3536572 |
BXGD019065 |
End stage renal disease due to hypertension |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Cardiovascular Diseases |
| C3536740 |
BXGD019073 |
Cervical meningomyelocele |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C3539878 |
BXGD019087 |
Triple Negative Breast Neoplasms |
Neoplasms; Skin and Connective Tissue Diseases |
| C3550150 |
BXGD019132 |
Recurrent thrombophlebitis |
Cardiovascular Diseases |
| C3647902 |
BXGD019250 |
Vasculogenic erectile dysfunction |
Male Urogenital Diseases; Mental Disorders |
| C3658290 |
BXGD019256 |
Drug-Induced Acute Liver Injury |
Digestive System Diseases; Chemically-Induced Disorders |
| C3662483 |
BXGD019270 |
Allergic sensitization |
|
| C3665816 |
BXGD019306 |
Perinatal stroke |
|
| C3714514 |
BXGD019409 |
Infection |
Infections |
| C3714542 |
BXGD019413 |
Lymphoma, Diffuse |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C3714636 |
BXGD019421 |
Pneumonitis |
Infections; Respiratory Tract Diseases |
| C3714756 |
BXGD019429 |
Intellectual Disability |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C3714757 |
BXGD019430 |
Juvenile rheumatoid arthritis |
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases |
| C3805043 |
BXGD019457 |
Vascular cognitive impairment |
|
| C3805092 |
BXGD019461 |
Methylenetetrahydrofolate reductase gene mutation |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C3806347 |
BXGD019506 |
Hyperhomocystinemia |
|
| C3811653 |
BXGD019662 |
Experimental Organism Basal Cell Carcinoma |
Neoplasms |
| C3824874 |
BXGD019679 |
Mycoplasma pneumoniae Infection |
Infections; Respiratory Tract Diseases |
| C3825293 |
BXGD019689 |
Headache in children |
|
| C3826044 |
BXGD019710 |
Lymphoblastic leukemia in children |
|
| C3826462 |
BXGD019725 |
Depression in children |
|
| C3843752 |
BXGD019804 |
Asthma, doctor diagnosed |
|
| C3887461 |
BXGD019876 |
Head and Neck Carcinoma |
Neoplasms |
| C3887641 |
BXGD019909 |
Recurrent hepatitis |
Digestive System Diseases |
| C3891448 |
BXGD020030 |
NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO |
|
| C4017062 |
BXGD020398 |
HOMOCYSTINURIA DUE TO MTHFR DEFICIENCY |
|
| C4021107 |
BXGD020557 |
Non-obstructive azoospermia |
Male Urogenital Diseases |
| C4021768 |
BXGD020766 |
Abnormality of metabolism/homeostasis |
|
| C4021813 |
BXGD020799 |
Oral cleft |
|
| C4023106 |
BXGD021109 |
Obstructive azoospermia |
Male Urogenital Diseases |
| C4024896 |
BXGD021461 |
Motor neuron atrophy |
|
| C4024948 |
BXGD021495 |
Anterior encephalocele |
|
| C4048328 |
BXGD021903 |
cervical cancer |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications |
| C4048329 |
BXGD021904 |
Immunosuppression |
|
| C4049272 |
BXGD021918 |
Tumour budding |
|
| C4083212 |
BXGD022105 |
Alopecia, Male Pattern |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases |
| C4086165 |
BXGD022126 |
Childhood Neuroblastoma |
Neoplasms |
| C4237343 |
BXGD022309 |
Overweight or obesity |
|
| C4275242 |
BXGD022371 |
Sudden sensorineural hearing loss |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases |
| C4277682 |
BXGD022376 |
Chemical and Drug Induced Liver Injury |
Digestive System Diseases; Chemically-Induced Disorders |
| C4279912 |
BXGD022378 |
Chemically-Induced Liver Toxicity |
Digestive System Diseases; Chemically-Induced Disorders |
| C4302205 |
BXGD022530 |
Neonatal thrombosis of cerebral venous sinus |
|
| C4303479 |
BXGD022561 |
Homocystinuria without methylmalonic aciduria |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Nervous System Diseases |
| C4317091 |
BXGD022722 |
Trisomy 18 Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C4321245 |
BXGD022744 |
Cleft lip or lips |
|
| C4321477 |
BXGD022752 |
Sickle Cell-SS Disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C4324584 |
BXGD022773 |
Periprocedural myocardial infarction |
|
| C4324656 |
BXGD022775 |
Non-squamous non-small cell lung cancer |
Neoplasms; Respiratory Tract Diseases |
| C4511452 |
BXGD023002 |
Sporadic Parkinson disease |
Nervous System Diseases |
| C4521042 |
BXGD023055 |
Complete Trisomy 21 Syndrome |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C4525124 |
BXGD023120 |
Stage III Colon Cancer AJCC v8 |
|
| C4525128 |
BXGD023122 |
Stage IV Colon Cancer AJCC v8 |
|
| 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 |
|
| C4551538 |
BXGD023340 |
refractory multiple myeloma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases |
| C4551686 |
BXGD023391 |
Malignant neoplasm of soft tissue |
Neoplasms |
| C4551915 |
BXGD023441 |
Gait Disturbance, CTCAE |
|
| C4552100 |
BXGD023488 |
Lynch Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Nutritional and Metabolic Diseases |
| C4552318 |
BXGD023501 |
Gastrointestinal adenocarcinoma |
|
| C4552766 |
BXGD023523 |
Miscarriage |
Female Urogenital Diseases and Pregnancy Complications |
| C4688308 |
BXGD023583 |
Advanced Lung Non-Squamous Non-Small Cell Carcinoma |
|
| C4699508 |
BXGD023637 |
Cardioembolism (high-risk/medium-risk) |
|
| C4704874 |
BXGD023682 |
Mammary Carcinoma, Human |
Neoplasms; Skin and Connective Tissue Diseases |
| C4721453 |
BXGD023744 |
Peripheral Nervous System Diseases |
Nervous System Diseases |
| C4721532 |
BXGD023752 |
Lymphoma, Non-Hodgkin, Familial |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C4721579 |
BXGD023759 |
Secondary malignant neoplasm of colon and/or rectum |
Digestive System Diseases; Neoplasms |
| C4721610 |
BXGD023760 |
Carcinoma, Ovarian Epithelial |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C4721806 |
BXGD023772 |
Carcinoma, Basal Cell |
Neoplasms |
| C4722085 |
BXGD023788 |
Malignant neoplasm of colon and/or rectum |
|
| C4722099 |
BXGD023789 |
High grade glioma |
Neoplasms |
| C4722419 |
BXGD023802 |
Extrapulmonary Small Cell Carcinoma |
Neoplasms |
| C4722518 |
BXGD023806 |
Triple-Negative Breast Carcinoma |
Neoplasms; Skin and Connective Tissue Diseases |
