| C0001363 |
BXGD000046 |
Acute vascular insufficiency of intestine (disorder) |
Digestive System Diseases |
| C0002170 |
BXGD000105 |
Alopecia |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases |
| C0002395 |
BXGD000111 |
Alzheimer's Disease |
Nervous System Diseases; Mental Disorders |
| C0002963 |
BXGD000161 |
Angina Pectoris, Variant |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0003467 |
BXGD000194 |
Anxiety |
Behavior and Behavior Mechanisms |
| C0003469 |
BXGD000195 |
Anxiety Disorders |
Mental Disorders |
| C0003486 |
BXGD000197 |
Aortic Aneurysm |
Cardiovascular Diseases |
| C0003509 |
BXGD000204 |
Aortitis |
Cardiovascular Diseases |
| C0003615 |
BXGD000212 |
Appendicitis |
Digestive System Diseases; Infections |
| C0003811 |
BXGD000222 |
Cardiac Arrhythmia |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0003857 |
BXGD000228 |
Congenital arteriovenous malformation |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C0003873 |
BXGD000236 |
Rheumatoid Arthritis |
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases |
| C0004106 |
BXGD000254 |
Astigmatism |
Eye Diseases |
| C0004134 |
BXGD000256 |
Ataxia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0004238 |
BXGD000262 |
Atrial Fibrillation |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0005695 |
BXGD000323 |
Bladder Neoplasm |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0005699 |
BXGD000325 |
Blast Phase |
Pathological Conditions, Signs and Symptoms; Neoplasms; Hemic and Lymphatic Diseases |
| C0005941 |
BXGD000353 |
Bone Diseases, Developmental |
Musculoskeletal Diseases |
| C0006118 |
BXGD000372 |
Brain Neoplasms |
Neoplasms; Nervous System Diseases |
| C0006826 |
BXGD000408 |
Malignant Neoplasms |
Neoplasms |
| C0007102 |
BXGD000425 |
Malignant tumor of colon |
Digestive System Diseases; Neoplasms |
| C0007137 |
BXGD000445 |
Squamous cell carcinoma |
Neoplasms |
| C0007177 |
BXGD000449 |
Cardiac Tamponade |
Cardiovascular Diseases |
| C0007193 |
BXGD000451 |
Cardiomyopathy, Dilated |
Cardiovascular Diseases |
| C0007282 |
BXGD000458 |
Carotid Stenosis |
Nervous System Diseases; Cardiovascular Diseases |
| C0007758 |
BXGD000475 |
Cerebellar Ataxia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0007766 |
BXGD000478 |
Intracranial Aneurysm |
Nervous System Diseases; Cardiovascular Diseases |
| C0007785 |
BXGD000485 |
Cerebral Infarction |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases |
| C0008031 |
BXGD000511 |
Chest Pain |
Pathological Conditions, Signs and Symptoms |
| C0008626 |
BXGD000559 |
Congenital chromosomal disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C0009398 |
BXGD000604 |
Color vision defect |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C0009402 |
BXGD000605 |
Colorectal Carcinoma |
Digestive System Diseases; Neoplasms |
| C0009782 |
BXGD000631 |
Connective Tissue Diseases |
Skin and Connective Tissue Diseases |
| C0010054 |
BXGD000647 |
Coronary Arteriosclerosis |
Cardiovascular Diseases |
| C0010068 |
BXGD000648 |
Coronary heart disease |
Cardiovascular Diseases |
| C0011847 |
BXGD000749 |
Diabetes |
Endocrine System Diseases |
| C0011849 |
BXGD000751 |
Diabetes Mellitus |
Nutritional and Metabolic Diseases; Endocrine System Diseases |
| C0011860 |
BXGD000755 |
Diabetes Mellitus, Non-Insulin-Dependent |
Nutritional and Metabolic Diseases; Endocrine System Diseases |
| C0013080 |
BXGD000797 |
Down Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0013336 |
BXGD000815 |
Dwarfism |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases |
| C0013362 |
BXGD000817 |
Dysarthria |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0014065 |
BXGD000884 |
Congenital cerebral hernia |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0014116 |
BXGD000892 |
Endocardial Cushion Defects |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C0014121 |
BXGD000895 |
Bacterial Endocarditis |
Infections; Cardiovascular Diseases |
| C0014859 |
BXGD000961 |
Esophageal Neoplasms |
Digestive System Diseases; Neoplasms |
| C0016052 |
BXGD001040 |
Fibromuscular Dysplasia |
Cardiovascular Diseases |
| C0016053 |
BXGD001041 |
Fibromyalgia |
Musculoskeletal Diseases; Nervous System Diseases |
| C0016169 |
BXGD001048 |
pathologic fistula |
Pathological Conditions, Signs and Symptoms |
| C0017636 |
BXGD001131 |
Glioblastoma |
Neoplasms |
| C0018213 |
BXGD001187 |
Graves Disease |
Eye Diseases; Immune System Diseases; Endocrine System Diseases |
| C0018671 |
BXGD001211 |
Head and Neck Neoplasms |
Neoplasms |
| C0018817 |
BXGD001235 |
Atrial Septal Defects |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| 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 |
| C0020538 |
BXGD001422 |
Hypertensive disease |
Cardiovascular Diseases |
| C0021933 |
BXGD001524 |
Intussusception |
Digestive System Diseases |
| C0022578 |
BXGD001557 |
Keratoconus |
Eye Diseases |
| C0022660 |
BXGD001571 |
Kidney Failure, Acute |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0023434 |
BXGD001643 |
Chronic Lymphocytic Leukemia |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0023467 |
BXGD001658 |
Leukemia, Myelocytic, Acute |
Neoplasms |
| C0023470 |
BXGD001659 |
Myeloid Leukemia |
Neoplasms |
| C0023473 |
BXGD001661 |
Myeloid Leukemia, Chronic |
Neoplasms; Hemic and Lymphatic Diseases |
| C0023787 |
BXGD001698 |
Lipodystrophy |
Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases |
| C0024003 |
BXGD001726 |
Lordosis |
Musculoskeletal Diseases |
| C0024636 |
BXGD001793 |
Malocclusion |
Stomatognathic Diseases |
| C0025149 |
BXGD001826 |
Medulloblastoma |
Neoplasms |
| C0025202 |
BXGD001832 |
melanoma |
Neoplasms |
| C0026764 |
BXGD001928 |
Multiple Myeloma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases |
| C0026827 |
BXGD001936 |
Muscle hypotonia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0027022 |
BXGD001962 |
Myeloproliferative disease |
Hemic and Lymphatic Diseases |
| C0027051 |
BXGD001963 |
Myocardial Infarction |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0027092 |
BXGD001971 |
Myopia |
Eye Diseases |
| C0027651 |
BXGD002009 |
Neoplasms |
Neoplasms |
| C0028077 |
BXGD002069 |
Nyctalopia |
Eye Diseases |
| C0028738 |
BXGD002081 |
Nystagmus |
Eye Diseases; Nervous System Diseases |
| C0029463 |
BXGD002160 |
Osteosarcoma |
Neoplasms |
| C0030193 |
BXGD002191 |
Pain |
Pathological Conditions, Signs and Symptoms |
| C0032131 |
BXGD002330 |
Plasmacytoma |
Neoplasms; Immune System Diseases |
| C0033999 |
BXGD002448 |
Pterygium |
Eye Diseases |
| C0036341 |
BXGD002600 |
Schizophrenia |
Mental Disorders |
| C0036439 |
BXGD002615 |
Scoliosis, unspecified |
Musculoskeletal Diseases |
| C0036572 |
BXGD002625 |
Seizures |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0038219 |
BXGD002739 |
Status Dysraphicus |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0038454 |
BXGD002760 |
Cerebrovascular accident |
Nervous System Diseases; Cardiovascular Diseases |
| C0038529 |
BXGD002769 |
Subchondral Cysts |
Neoplasms; Musculoskeletal 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 |
| C0079744 |
BXGD003090 |
Diffuse Large B-Cell Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0080178 |
BXGD003107 |
Spina Bifida |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0085096 |
BXGD003123 |
Peripheral Vascular Diseases |
Cardiovascular Diseases |
| C0085281 |
BXGD003152 |
Addictive Behavior |
Behavior and Behavior Mechanisms |
| C0085636 |
BXGD003218 |
Photophobia |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C0086543 |
BXGD003294 |
Cataract |
Eye Diseases |
| C0151517 |
BXGD003431 |
Complete atrioventricular block |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0151744 |
BXGD003469 |
Myocardial Ischemia |
Cardiovascular Diseases |
| C0152018 |
BXGD003518 |
Esophageal carcinoma |
Digestive System Diseases; Neoplasms |
| C0152164 |
BXGD003550 |
Cyclical vomiting syndrome (disorder) |
Pathological Conditions, Signs and Symptoms |
| C0153594 |
BXGD003669 |
Malignant neoplasm of testis |
Neoplasms; Male Urogenital Diseases; Endocrine System Diseases |
| C0153676 |
BXGD003679 |
Secondary malignant neoplasm of lung |
Neoplasms; Respiratory Tract Diseases |
| C0154920 |
BXGD003755 |
Pigmentary iris degeneration |
Eye Diseases; Skin and Connective Tissue Diseases |
| C0158623 |
BXGD003894 |
Congenital anomaly of coronary artery |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C0162298 |
BXGD003933 |
Joint stiffness |
Musculoskeletal Diseases |
| C0162871 |
BXGD003996 |
Aortic Aneurysm, Abdominal |
Cardiovascular Diseases |
| C0205851 |
BXGD004132 |
Germ cell tumor |
Neoplasms |
| C0206180 |
BXGD004170 |
Ki-1+ Anaplastic Large Cell Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0206754 |
BXGD004289 |
Neuroendocrine Tumors |
Neoplasms |
| C0221032 |
BXGD004374 |
Familial generalized lipodystrophy |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases |
| C0221357 |
BXGD004449 |
Brachydactyly |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0235974 |
BXGD004796 |
Pancreatic carcinoma |
Digestive System Diseases; Neoplasms; Endocrine System Diseases |
| C0238045 |
BXGD004863 |
Carotid-Cavernous Sinus Fistula |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases; Wounds and Injuries |
| C0238463 |
BXGD004938 |
Papillary thyroid carcinoma |
Neoplasms; Endocrine System Diseases |
| C0239138 |
BXGD004966 |
Hip joint varus deformity - observation |
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases |
| C0239594 |
BXGD004987 |
Short finger |
|
| C0241688 |
BXGD005107 |
Peripheral visual field loss |
|
| C0242231 |
BXGD005144 |
Coronary Stenosis |
Cardiovascular Diseases |
| C0242350 |
BXGD005154 |
Erectile dysfunction |
Male Urogenital Diseases; Mental Disorders |
| C0242363 |
BXGD005156 |
Islet Cell Tumor |
Digestive System Diseases; Neoplasms; Endocrine System Diseases |
| C0242379 |
BXGD005157 |
Malignant neoplasm of lung |
Neoplasms; Respiratory Tract Diseases |
| C0265101 |
BXGD005454 |
Carotid artery occlusion |
Nervous System Diseases; Cardiovascular Diseases |
| C0265509 |
BXGD005540 |
Congenital anomaly of skeletal bone |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases |
| C0266508 |
BXGD005684 |
Rachischisis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0278510 |
BXGD006526 |
Childhood Medulloblastoma |
Neoplasms |
| C0278876 |
BXGD006607 |
Adult Medulloblastoma |
Neoplasms |
| C0280100 |
BXGD006713 |
Solid Neoplasm |
Neoplasms |
| C0333307 |
BXGD006946 |
Superficial ulcer |
Pathological Conditions, Signs and Symptoms |
| C0339527 |
BXGD007260 |
Leber Congenital Amaurosis |
Eye Diseases |
| C0340288 |
BXGD007316 |
Stable angina |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0340517 |
BXGD007339 |
Atrial thrombosis |
|
| C0340629 |
BXGD007354 |
Aortic aneurysm without mention of rupture NOS |
Cardiovascular Diseases |
| C0340647 |
BXGD007358 |
Distal aortic dissection |
|
| C0340896 |
BXGD007372 |
Vascular graft infection |
Pathological Conditions, Signs and Symptoms; Infections; Cardiovascular Diseases |
| C0342500 |
BXGD007492 |
Adrenal mass |
Endocrine System Diseases |
| C0345905 |
BXGD007746 |
Intrahepatic Cholangiocarcinoma |
Neoplasms |
| C0346647 |
BXGD007832 |
Malignant neoplasm of pancreas |
Digestive System Diseases; Neoplasms; Endocrine System Diseases |
| C0375206 |
BXGD007973 |
Hemiplegia/hemiparesis |
|
| C0376358 |
BXGD007992 |
Malignant neoplasm of prostate |
Neoplasms; Male Urogenital Diseases |
| C0376545 |
BXGD008002 |
Hematologic Neoplasms |
Neoplasms; Hemic and Lymphatic Diseases |
| C0409959 |
BXGD008400 |
Osteoarthritis, Knee |
Musculoskeletal Diseases |
| C0410653 |
BXGD008444 |
Atlantoaxial instability |
|
| C0476397 |
BXGD008991 |
Electroretinogram abnormal |
|
| C0494165 |
BXGD009022 |
Secondary malignant neoplasm of liver |
Digestive System Diseases; Neoplasms |
| C0520680 |
BXGD009102 |
Sleep Apnea, Central |
Respiratory Tract Diseases; Nervous System Diseases |
| C0524620 |
BXGD009236 |
Metabolic Syndrome X |
Nutritional and Metabolic Diseases |
| C0543822 |
BXGD009296 |
Atherosclerotic occlusive disease |
Cardiovascular Diseases |
| C0546837 |
BXGD009343 |
Malignant neoplasm of esophagus |
Digestive System Diseases; Neoplasms |
| C0557874 |
BXGD009444 |
Global developmental delay |
|
| C0566888 |
BXGD009493 |
Narrow sacrosciatic notch |
|
| C0585442 |
BXGD009593 |
Osteosarcoma of bone |
Neoplasms |
| C0596263 |
BXGD009639 |
Carcinogenesis |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0600139 |
BXGD009695 |
Prostate carcinoma |
Neoplasms; Male Urogenital Diseases |
| C0677607 |
BXGD009721 |
Hashimoto Disease |
Endocrine System Diseases |
| C0684249 |
BXGD009790 |
Carcinoma of lung |
Neoplasms; Respiratory Tract Diseases |
| C0699790 |
BXGD009866 |
Colon Carcinoma |
Digestive System Diseases; Neoplasms |
| C0700635 |
BXGD009897 |
Strudwick syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0742343 |
BXGD010061 |
Acute Chest Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Hemic and Lymphatic Diseases |
| C0747085 |
BXGD010158 |
Recurrent otitis media |
Otorhinolaryngologic Diseases |
| C0751039 |
BXGD010302 |
Cockayne Syndrome, Type I |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases |
| C0751559 |
BXGD010500 |
Pulsatile Tinnitus |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases |
| C0751688 |
BXGD010551 |
Malignant Squamous Cell Neoplasm |
Neoplasms |
| C0751956 |
BXGD010653 |
Acute Cerebrovascular Accidents |
Nervous System Diseases; Cardiovascular Diseases |
| C0752143 |
BXGD010675 |
Intracranial Thrombosis |
Nervous System Diseases; Cardiovascular Diseases |
| C0752156 |
BXGD010680 |
Dural Arteriovenous Fistula |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases |
| C0752304 |
BXGD010711 |
Hypoxic-Ischemic Encephalopathy |
Nervous System Diseases; Cardiovascular Diseases |
| C0854723 |
BXGD011026 |
Retinal Dystrophies |
Eye Diseases |
| C0860207 |
BXGD011220 |
Drug-Induced Liver Disease |
Digestive System Diseases; Chemically-Induced Disorders |
| C0917804 |
BXGD011413 |
Arteriovenous Malformations, Cerebral |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases |
| C0917996 |
BXGD011425 |
Cerebral Aneurysm |
Nervous System Diseases; Cardiovascular Diseases |
| C0919267 |
BXGD011426 |
ovarian neoplasm |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C0948008 |
BXGD011499 |
Ischemic stroke |
Nervous System Diseases; Cardiovascular Diseases |
| C0948089 |
BXGD011504 |
Acute Coronary Syndrome |
Cardiovascular Diseases |
| C1140680 |
BXGD011718 |
Malignant neoplasm of ovary |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C1262760 |
BXGD011886 |
Hepatitis, Drug-Induced |
Digestive System Diseases; Chemically-Induced Disorders |
| C1265768 |
BXGD011920 |
Calcified aneurysm |
Cardiovascular Diseases |
| C1292778 |
BXGD012237 |
Chronic myeloproliferative disorder |
Neoplasms; Hemic and Lymphatic Diseases |
| C1306459 |
BXGD012361 |
Primary malignant neoplasm |
Neoplasms |
| C1306460 |
BXGD012362 |
Primary malignant neoplasm of lung |
Neoplasms; Respiratory Tract Diseases |
| C1306889 |
BXGD012380 |
Peripheral arterial occlusive disease |
Cardiovascular Diseases |
| C1319315 |
BXGD012415 |
Adenocarcinoma of large intestine |
Digestive System Diseases; Neoplasms |
| C1332986 |
BXGD012574 |
Childhood Osteosarcoma |
Neoplasms |
| C1337011 |
BXGD012874 |
Well Differentiated Pancreatic Endocrine Tumor |
Digestive System Diseases; Neoplasms; Endocrine System Diseases |
| C1384666 |
BXGD012948 |
hearing impairment |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases |
| C1402315 |
BXGD013017 |
Vascular lesions |
|
| C1412000 |
BXGD013049 |
Mesenteric vascular insufficiency |
Digestive System Diseases; Cardiovascular Diseases |
| C1510586 |
BXGD013176 |
Autism Spectrum Disorders |
Mental Disorders |
| C1536220 |
BXGD013341 |
ST segment elevation myocardial infarction |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C1541923 |
BXGD013355 |
Infective endocarditis |
Cardiovascular Diseases |
| C1561643 |
BXGD013363 |
Chronic Kidney Diseases |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C1611743 |
BXGD013456 |
Familial (FPAH) |
|
| C1621958 |
BXGD013468 |
Glioblastoma Multiforme |
Neoplasms |
| C1704436 |
BXGD013564 |
Peripheral Arterial Diseases |
Cardiovascular Diseases |
| C1707444 |
BXGD013586 |
Columnar Cell Change of the Breast |
|
| C1836589 |
BXGD014135 |
Decreased hip abduction |
|
| C1837073 |
BXGD014191 |
Spondylometaphyseal Dysplasia with Cone-Rod Dystrophy |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Musculoskeletal Diseases |
| C1837078 |
BXGD014192 |
Hypoplastic inferior ilia |
|
| C1837081 |
BXGD014193 |
Tibial bowing |
Musculoskeletal Diseases |
| C1837082 |
BXGD014194 |
Metaphyseal cupping |
|
| C1837084 |
BXGD014195 |
Short metacarpal |
|
| C1837249 |
BXGD014210 |
Malformations of Cortical Development, Group II |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C1837454 |
BXGD014232 |
SPINOCEREBELLAR ATAXIA 8 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C1838662 |
BXGD014334 |
Metaphyseal irregularity |
|
| C1839364 |
BXGD014371 |
Progressive visual loss |
|
| C1842083 |
BXGD014494 |
Abnormality of the ribs |
|
| C1842937 |
BXGD014546 |
AURAL ATRESIA, CONGENITAL |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C1843108 |
BXGD014556 |
Short palm |
|
| C1844548 |
BXGD014642 |
Hypoplastic finger |
|
| C1844704 |
BXGD014665 |
Platyspondyly |
|
| C1849039 |
BXGD014999 |
Metaphyseal widening |
|
| C1849955 |
BXGD015094 |
Limited elbow movement |
|
| C1850293 |
BXGD015126 |
Severe platyspondyly |
|
| C1855340 |
BXGD015490 |
Bowing of the long bones |
|
| C1855665 |
BXGD015524 |
Ovoid vertebral bodies |
|
| C1855676 |
BXGD015528 |
Aplasia/Hypoplasia of the cerebellar vermis |
|
| C1855925 |
BXGD015561 |
Hyperopia, High |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C1859461 |
BXGD015895 |
Femoral bowing |
Musculoskeletal Diseases |
| C1859778 |
BXGD015931 |
Postnatal growth retardation |
|
| C1862389 |
BXGD016126 |
ATRIAL SEPTAL DEFECT 1 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C1862475 |
BXGD016132 |
Abnormality of retinal pigmentation |
|
| C1865039 |
BXGD016291 |
Cupped ribs |
|
| C1866730 |
BXGD016419 |
Rhizomelia |
|
| C1867441 |
BXGD016455 |
Pterygium Of Conjunctiva And Cornea |
Eye Diseases |
| C1868737 |
BXGD016533 |
Vertebral artery hypoplasia |
|
| C1956346 |
BXGD016627 |
Coronary Artery Disease |
Cardiovascular Diseases |
| C1963184 |
BXGD016688 |
Nystagmus, CTCAE 3.0 |
|
| C2239176 |
BXGD016965 |
Liver carcinoma |
Digestive System Diseases; Neoplasms |
| C2882221 |
BXGD017842 |
Acute pulmonary embolism |
Respiratory Tract Diseases; Cardiovascular Diseases |
| C2931019 |
BXGD017938 |
Split hand foot deformity 1 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C2936351 |
BXGD018111 |
Fibroatheroma |
Pathological Conditions, Signs and Symptoms |
| C3203102 |
BXGD018555 |
Idiopathic pulmonary arterial hypertension |
Respiratory Tract Diseases |
| C3275069 |
BXGD018658 |
Chronic Total Occlusion Vessel |
|
| C3658290 |
BXGD019256 |
Drug-Induced Acute Liver Injury |
Digestive System Diseases; Chemically-Induced Disorders |
| C3665346 |
BXGD019278 |
Unspecified visual loss |
Pathological Conditions, Signs and Symptoms; Eye Diseases |
| C3665347 |
BXGD019279 |
Visual Impairment |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C3665365 |
BXGD019282 |
Arteriosclerotic cardiovascular disease, NOS |
Cardiovascular Diseases |
| C3665386 |
BXGD019284 |
Abnormal vision |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C3714756 |
BXGD019429 |
Intellectual Disability |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C3808249 |
BXGD019541 |
Abnormality of the optic disc |
|
| C3809715 |
BXGD019607 |
Spontaneous, recurrent epistaxis |
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Otorhinolaryngologic Diseases |
| C3840565 |
BXGD019797 |
Autoimmune thyroid disease (AITD) |
|
| C3887524 |
BXGD019892 |
Skin Erosion |
Skin and Connective Tissue Diseases |
| C3898139 |
BXGD020062 |
New or Worsening Symptom |
|
| C4024756 |
BXGD021405 |
Abnormality of macular pigmentation |
|
| C4025787 |
BXGD021788 |
Calvarial skull defect |
|
| C4025800 |
BXGD021797 |
Large central visual field defect |
|
| C4085590 |
BXGD022119 |
Cone-Rod Dystrophies |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye 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 |
| C4284013 |
BXGD022428 |
Primary cholangiocarcinoma of intrahepatic biliary tract |
Neoplasms |
| C4476910 |
BXGD022887 |
Thin-cap fibroatheroma |
Cardiovascular Diseases |
| C4520843 |
BXGD023043 |
Pterygium of eye |
Eye Diseases |
| C4521042 |
BXGD023055 |
Complete Trisomy 21 Syndrome |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C4552000 |
BXGD023473 |
Episodic Kinesigenic Dyskinesia 1 |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C4554036 |
BXGD023557 |
Nystagmus, CTCAE 5.0 |
|
| C4703473 |
BXGD023650 |
Atherosclerotic lesion |
Cardiovascular Diseases |
| C4703564 |
BXGD023659 |
Aortopulmonary collateral arteries |
|
| C4721610 |
BXGD023760 |
Carcinoma, Ovarian Epithelial |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C4722085 |
BXGD023788 |
Malignant neoplasm of colon and/or rectum |
|
