| C0001418 |
BXGD000050 |
Adenocarcinoma |
Neoplasms |
| C0002726 |
BXGD000125 |
Amyloidosis |
Nutritional and Metabolic Diseases |
| C0002895 |
BXGD000152 |
Anemia, Sickle Cell |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0002962 |
BXGD000160 |
Angina Pectoris |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0002982 |
BXGD000163 |
Angioid Streaks |
Eye Diseases |
| C0003850 |
BXGD000225 |
Arteriosclerosis |
Cardiovascular Diseases |
| C0003873 |
BXGD000236 |
Rheumatoid Arthritis |
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases |
| C0004153 |
BXGD000260 |
Atherosclerosis |
Cardiovascular Diseases |
| C0005283 |
BXGD000308 |
beta Thalassemia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0005779 |
BXGD000336 |
Blood Coagulation Disorders |
Hemic and Lymphatic Diseases |
| C0005890 |
BXGD000345 |
Body Height |
|
| C0007134 |
BXGD000443 |
Renal Cell Carcinoma |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0007196 |
BXGD000453 |
Restrictive cardiomyopathy |
Cardiovascular Diseases |
| C0007222 |
BXGD000454 |
Cardiovascular Diseases |
Cardiovascular Diseases |
| C0007570 |
BXGD000467 |
Celiac Disease |
Digestive System Diseases; Nutritional and Metabolic Diseases |
| C0008312 |
BXGD000527 |
Primary biliary cirrhosis |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C0009402 |
BXGD000605 |
Colorectal Carcinoma |
Digestive System Diseases; Neoplasms |
| C0009404 |
BXGD000606 |
Colorectal Neoplasms |
Digestive System Diseases; Neoplasms |
| C0009782 |
BXGD000631 |
Connective Tissue Diseases |
Skin and Connective Tissue Diseases |
| C0010054 |
BXGD000647 |
Coronary Arteriosclerosis |
Cardiovascular Diseases |
| C0010068 |
BXGD000648 |
Coronary heart disease |
Cardiovascular Diseases |
| C0010495 |
BXGD000674 |
Cutis Laxa |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases |
| C0011644 |
BXGD000744 |
Scleroderma |
Skin and Connective Tissue Diseases |
| C0011881 |
BXGD000760 |
Diabetic Nephropathy |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases |
| C0014772 |
BXGD000948 |
Red Blood Cell Count measurement |
|
| C0015230 |
BXGD000969 |
Exanthema |
Skin and Connective Tissue Diseases |
| C0015934 |
BXGD001026 |
Fetal Growth Retardation |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications |
| C0017181 |
BXGD001103 |
Gastrointestinal Hemorrhage |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C0017638 |
BXGD001132 |
Glioma |
Neoplasms |
| C0018213 |
BXGD001187 |
Graves Disease |
Eye Diseases; Immune System Diseases; Endocrine System Diseases |
| C0018802 |
BXGD001227 |
Congestive heart failure |
Cardiovascular Diseases |
| C0019045 |
BXGD001269 |
Hemoglobinopathies |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0019163 |
BXGD001295 |
Hepatitis B |
Digestive System Diseases; Infections |
| C0019189 |
BXGD001298 |
Hepatitis, Chronic |
Digestive System Diseases |
| C0019196 |
BXGD001301 |
Hepatitis C |
Digestive System Diseases; Infections |
| C0019829 |
BXGD001350 |
Hodgkin Disease |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0020295 |
BXGD001372 |
Hydronephrosis |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0020538 |
BXGD001422 |
Hypertensive disease |
Cardiovascular Diseases |
| C0020626 |
BXGD001452 |
Hypoparathyroidism |
Endocrine System Diseases |
| C0020676 |
BXGD001462 |
Hypothyroidism |
Endocrine System Diseases |
| C0020758 |
BXGD001467 |
Congenital ichthyosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases |
| C0021775 |
BXGD001512 |
Intermittent Claudication |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0022350 |
BXGD001538 |
Jaundice, Chronic Idiopathic |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0022573 |
BXGD001554 |
Keratoconjunctivitis |
Eye Diseases |
| C0022821 |
BXGD001590 |
Kyphosis deformity of spine |
Musculoskeletal Diseases |
| C0023418 |
BXGD001642 |
leukemia |
Neoplasms |
| C0023467 |
BXGD001658 |
Leukemia, Myelocytic, Acute |
Neoplasms |
| C0023473 |
BXGD001661 |
Myeloid Leukemia, Chronic |
Neoplasms; Hemic and Lymphatic Diseases |
| C0023530 |
BXGD001683 |
Leukopenia |
Hemic and Lymphatic Diseases |
| C0023895 |
BXGD001717 |
Liver diseases |
Digestive System Diseases |
| C0024138 |
BXGD001738 |
Lupus Erythematosus, Discoid |
Skin and Connective Tissue Diseases |
| C0024141 |
BXGD001740 |
Lupus Erythematosus, Systemic |
Skin and Connective Tissue Diseases; Immune System Diseases |
| C0025312 |
BXGD001861 |
Meningomyelocele |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0025517 |
BXGD001875 |
Metabolic Diseases |
Nutritional and Metabolic Diseases |
| C0026267 |
BXGD001896 |
Mitral Valve Prolapse Syndrome |
Cardiovascular Diseases |
| C0026269 |
BXGD001897 |
Mitral Valve Stenosis |
Cardiovascular Diseases |
| C0026633 |
BXGD001910 |
Mouth Abnormalities |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases |
| C0026654 |
BXGD001914 |
Moyamoya Disease |
Nervous System Diseases; Cardiovascular Diseases |
| C0026896 |
BXGD001946 |
Myasthenia Gravis |
Neoplasms; Immune System Diseases; Nervous System Diseases |
| C0027051 |
BXGD001963 |
Myocardial Infarction |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0027092 |
BXGD001971 |
Myopia |
Eye Diseases |
| C0027651 |
BXGD002009 |
Neoplasms |
Neoplasms |
| C0027709 |
BXGD002026 |
Nephrocalcinosis |
Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0027947 |
BXGD002061 |
Neutropenia |
Hemic and Lymphatic Diseases |
| C0028754 |
BXGD002082 |
Obesity |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases |
| C0029456 |
BXGD002157 |
Osteoporosis |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C0030193 |
BXGD002191 |
Pain |
Pathological Conditions, Signs and Symptoms |
| C0030793 |
BXGD002253 |
Pelvic Neoplasms |
Neoplasms |
| C0031069 |
BXGD002279 |
Familial Mediterranean Fever |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C0031117 |
BXGD002285 |
Peripheral Neuropathy |
Nervous System Diseases |
| C0033774 |
BXGD002419 |
Pruritus |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases |
| C0033847 |
BXGD002437 |
Pseudoxanthoma Elasticum |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases |
| C0035309 |
BXGD002530 |
Retinal Diseases |
Eye Diseases |
| C0035317 |
BXGD002533 |
Retinal Hemorrhage |
Pathological Conditions, Signs and Symptoms; Eye Diseases |
| C0035334 |
BXGD002539 |
Retinitis Pigmentosa |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C0036421 |
BXGD002613 |
Systemic Scleroderma |
Skin and Connective Tissue Diseases |
| C0036439 |
BXGD002615 |
Scoliosis, unspecified |
Musculoskeletal Diseases |
| C0036572 |
BXGD002625 |
Seizures |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0037274 |
BXGD002676 |
Dermatologic disorders |
Skin and Connective Tissue Diseases |
| C0037772 |
BXGD002703 |
Spastic Paraplegia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0038449 |
BXGD002758 |
Stricture of artery |
Cardiovascular Diseases |
| C0038454 |
BXGD002760 |
Cerebrovascular accident |
Nervous System Diseases; Cardiovascular Diseases |
| C0042373 |
BXGD002978 |
Vascular Diseases |
Cardiovascular Diseases |
| C0042769 |
BXGD002999 |
Virus Diseases |
Infections |
| C0085096 |
BXGD003123 |
Peripheral Vascular Diseases |
Cardiovascular Diseases |
| C0085298 |
BXGD003155 |
Sudden Cardiac Death |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0085413 |
BXGD003171 |
Polycystic Kidney, Autosomal Dominant |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0151744 |
BXGD003469 |
Myocardial Ischemia |
Cardiovascular Diseases |
| C0151811 |
BXGD003478 |
Subcutaneous nodule |
Neoplasms; Skin and Connective Tissue Diseases; Musculoskeletal Diseases |
| C0151854 |
BXGD003487 |
Abnormal platelets |
Hemic and Lymphatic Diseases |
| C0152169 |
BXGD003551 |
Renal Colic |
Pathological Conditions, Signs and Symptoms |
| C0152459 |
BXGD003600 |
Linear atrophy |
Pathological Conditions, Signs and Symptoms |
| C0155626 |
BXGD003806 |
Acute myocardial infarction |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0162871 |
BXGD003996 |
Aortic Aneurysm, Abdominal |
Cardiovascular Diseases |
| C0206368 |
BXGD004176 |
Exfoliation Syndrome |
Eye Diseases |
| C0233514 |
BXGD004584 |
Abnormal behavior |
Behavior and Behavior Mechanisms |
| C0234632 |
BXGD004691 |
Reduced visual acuity |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C0235874 |
BXGD004781 |
Disease Exacerbation |
Pathological Conditions, Signs and Symptoms |
| C0240635 |
BXGD005047 |
Byzanthine arch palate |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Stomatognathic Diseases |
| C0241074 |
BXGD005078 |
Hyperextensible skin |
|
| C0241148 |
BXGD005081 |
Cutaneous plaque |
|
| C0242339 |
BXGD005150 |
Dyslipidemias |
Nutritional and Metabolic Diseases |
| C0242383 |
BXGD005160 |
Age related macular degeneration |
Eye Diseases |
| C0260037 |
BXGD005227 |
Multiple tumors |
Neoplasms |
| C0264955 |
BXGD005441 |
Idiopathic arterial calcification of infancy |
Nutritional and Metabolic Diseases; Cardiovascular Diseases |
| C0267446 |
BXGD005749 |
Acute gastroenteritis |
Digestive System Diseases |
| C0267602 |
BXGD005762 |
Descending perineum syndrome |
Digestive System Diseases |
| C0268307 |
BXGD005892 |
Conjugated hyperbilirubinemia |
Pathological Conditions, Signs and Symptoms |
| C0270685 |
BXGD006084 |
Cerebral calcification |
Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0271185 |
BXGD006170 |
Metamorphopsia |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C0271650 |
BXGD006227 |
Impaired glucose tolerance |
Nutritional and Metabolic Diseases |
| C0272315 |
BXGD006341 |
Coagulation factor deficiency syndrome |
Hemic and Lymphatic Diseases |
| C0332563 |
BXGD006894 |
Papule |
Pathological Conditions, Signs and Symptoms |
| C0333307 |
BXGD006946 |
Superficial ulcer |
Pathological Conditions, Signs and Symptoms |
| C0333440 |
BXGD006952 |
Hyaline body |
|
| C0342649 |
BXGD007522 |
Vascular calcification |
Nutritional and Metabolic Diseases |
| C0375206 |
BXGD007973 |
Hemiplegia/hemiparesis |
|
| C0376358 |
BXGD007992 |
Malignant neoplasm of prostate |
Neoplasms; Male Urogenital Diseases |
| C0376359 |
BXGD007993 |
Gronblad-Strandberg Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases |
| C0392525 |
BXGD008052 |
Nephrolithiasis |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0423798 |
BXGD008510 |
Increased tendency to bruise |
Wounds and Injuries |
| C0425791 |
BXGD008552 |
Peau d'orange surface of breast |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases |
| C0473583 |
BXGD008946 |
Nevus elasticus |
Neoplasms |
| C0497156 |
BXGD009053 |
Lymphadenopathy |
Hemic and Lymphatic Diseases |
| C0522055 |
BXGD009189 |
Electrocardiogram abnormal |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0524909 |
BXGD009247 |
Hepatitis B, Chronic |
Digestive System Diseases; Infections |
| C0542514 |
BXGD009277 |
Blue sclera |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C0553580 |
BXGD009399 |
Ewings sarcoma |
Neoplasms |
| C0557874 |
BXGD009444 |
Global developmental delay |
|
| C0600139 |
BXGD009695 |
Prostate carcinoma |
Neoplasms; Male Urogenital Diseases |
| C0600518 |
BXGD009711 |
Choroidal Neovascularization |
Pathological Conditions, Signs and Symptoms; Eye Diseases |
| C0685938 |
BXGD009829 |
Malignant neoplasm of gastrointestinal tract |
Digestive System Diseases; Neoplasms |
| C0702166 |
BXGD009912 |
Acne |
Skin and Connective Tissue Diseases |
| C0745730 |
BXGD010132 |
Multiple lipomata |
Neoplasms |
| C0877015 |
BXGD011327 |
Pelvic Organ Prolapse |
Pathological Conditions, Signs and Symptoms |
| C0948008 |
BXGD011499 |
Ischemic stroke |
Nervous System Diseases; Cardiovascular Diseases |
| C1168153 |
BXGD011780 |
Arterial calcification |
Nutritional and Metabolic Diseases |
| C1260959 |
BXGD011846 |
Drusen |
|
| C1269955 |
BXGD012005 |
Tumor Cell Invasion |
|
| C1301509 |
BXGD012294 |
Severe visual impairment |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C1397139 |
BXGD012995 |
Calcification of falx cerebri |
|
| C1397307 |
BXGD012996 |
Cardiac fibrosis |
|
| C1561643 |
BXGD013363 |
Chronic Kidney Diseases |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C1565489 |
BXGD013401 |
Renal Insufficiency |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C1611184 |
BXGD013455 |
Calcification of coronary artery |
Nutritional and Metabolic Diseases; Cardiovascular Diseases |
| C1688637 |
BXGD013488 |
Intraoperative floppy iris syndrome |
Pathological Conditions, Signs and Symptoms; Eye Diseases |
| C1704436 |
BXGD013564 |
Peripheral Arterial Diseases |
Cardiovascular Diseases |
| C1836940 |
BXGD014182 |
Thickened nuchal skin fold |
|
| C1837404 |
BXGD014229 |
High, narrow palate |
|
| C1842774 |
BXGD014536 |
Hypermelanotic macule |
|
| C1843921 |
BXGD014620 |
Postural instability |
Nervous System Diseases |
| C1849618 |
BXGD015072 |
Accelerated atherosclerosis |
Cardiovascular Diseases |
| C1859372 |
BXGD015882 |
Calcification of Joints and Arteries |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Cardiovascular Diseases |
| C1859727 |
BXGD015927 |
Arterial calcification of infancy |
Nutritional and Metabolic Diseases |
| C1860493 |
BXGD015987 |
Abnormality of the sternum |
|
| C1861502 |
BXGD016054 |
COLCHICINE RESISTANCE |
|
| C1867450 |
BXGD016457 |
Pseudoxanthoma Elasticum, Incomplete |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases |
| C1867451 |
BXGD016458 |
Pseudoxanthoma Elasticum, Heterozygous |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases |
| C1867453 |
BXGD016459 |
Peau d'orange retinal changes |
|
| C1867743 |
BXGD016470 |
Premature coronary artery atherosclerosis |
Cardiovascular Diseases |
| C1956346 |
BXGD016627 |
Coronary Artery Disease |
Cardiovascular Diseases |
| C1962966 |
BXGD016678 |
Retinopathy, CTCAE |
|
| C2033396 |
BXGD016889 |
Yellow papule |
|
| C2937358 |
BXGD018159 |
Cerebral Hemorrhage |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases |
| C3266262 |
BXGD018600 |
Multiple Chronic Conditions |
Pathological Conditions, Signs and Symptoms |
| C3276161 |
BXGD018684 |
ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 2 |
|
| C3553764 |
BXGD019187 |
Joint hyperflexibility |
|
| C3665347 |
BXGD019279 |
Visual Impairment |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C3841475 |
BXGD019800 |
beta^+^ Thalassemia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C3888506 |
BXGD019974 |
LDLR mutation |
|
| C3899278 |
BXGD020078 |
Early Rheumatoid Arthritis |
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases |
| C4021662 |
BXGD020726 |
Abnormal endocardium morphology |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C4021797 |
BXGD020787 |
Abnormality of the thorax |
|
| C4022001 |
BXGD020863 |
Abnormality of the cerebral vasculature |
|
| C4022018 |
BXGD020872 |
Telangiectasia of the skin |
Cardiovascular Diseases |
| C4022895 |
BXGD021030 |
Medial calcification of medium-sized arteries |
|
| C4024736 |
BXGD021396 |
Abnormally lax or hyperextensible skin |
|
| C4024890 |
BXGD021458 |
Excessive wrinkled skin |
|
| C4025265 |
BXGD021611 |
Medial calcification of large arteries |
|
| C4316870 |
BXGD022707 |
Abnormality of the eye |
|
| C4531299 |
BXGD023216 |
Premature occlusive vascular stenosis |
|
