| C0000731 |
BXGD000002 |
Abdomen distended |
Digestive System Diseases |
| C0000880 |
BXGD000016 |
Acanthamoeba Keratitis |
Infections; Eye Diseases |
| C0001418 |
BXGD000050 |
Adenocarcinoma |
Neoplasms |
| C0001430 |
BXGD000054 |
Adenoma |
Neoplasms |
| C0001973 |
BXGD000095 |
Alcoholic Intoxication, Chronic |
Chemically-Induced Disorders; Mental Disorders |
| C0002395 |
BXGD000111 |
Alzheimer's Disease |
Nervous System Diseases; Mental Disorders |
| C0002726 |
BXGD000125 |
Amyloidosis |
Nutritional and Metabolic Diseases |
| C0002792 |
BXGD000129 |
anaphylaxis |
Immune System Diseases |
| C0002871 |
BXGD000132 |
Anemia |
Hemic and Lymphatic Diseases |
| C0002949 |
BXGD000157 |
Aneurysm, Dissecting |
Cardiovascular Diseases |
| C0002965 |
BXGD000162 |
Angina, Unstable |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0002986 |
BXGD000165 |
Fabry Disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Cardiovascular Diseases |
| C0003467 |
BXGD000194 |
Anxiety |
Behavior and Behavior Mechanisms |
| C0003469 |
BXGD000195 |
Anxiety Disorders |
Mental Disorders |
| C0003477 |
BXGD000196 |
Separation Anxiety Disorder |
Mental Disorders |
| C0004096 |
BXGD000252 |
Asthma |
Respiratory Tract Diseases; Immune System Diseases |
| C0004134 |
BXGD000256 |
Ataxia |
Pathological Conditions, Signs and Symptoms; Nervous 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 |
| 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 |
| C0005779 |
BXGD000336 |
Blood Coagulation Disorders |
Hemic and Lymphatic Diseases |
| C0006111 |
BXGD000369 |
Brain Diseases |
Nervous System Diseases |
| C0006118 |
BXGD000372 |
Brain Neoplasms |
Neoplasms; Nervous System Diseases |
| C0006142 |
BXGD000374 |
Malignant neoplasm of breast |
Neoplasms; Skin and Connective Tissue Diseases |
| C0006826 |
BXGD000408 |
Malignant Neoplasms |
Neoplasms |
| C0007097 |
BXGD000424 |
Carcinoma |
Neoplasms |
| C0007102 |
BXGD000425 |
Malignant tumor of colon |
Digestive System Diseases; Neoplasms |
| C0007113 |
BXGD000430 |
Rectal Carcinoma |
Digestive System Diseases; Neoplasms |
| C0007115 |
BXGD000432 |
Malignant neoplasm of thyroid |
Neoplasms; Endocrine System Diseases |
| C0007222 |
BXGD000454 |
Cardiovascular Diseases |
Cardiovascular Diseases |
| C0007758 |
BXGD000475 |
Cerebellar Ataxia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0007789 |
BXGD000488 |
Cerebral Palsy |
Nervous System Diseases |
| C0007820 |
BXGD000491 |
Cerebrovascular Disorders |
Nervous System Diseases; Cardiovascular Diseases |
| C0007959 |
BXGD000507 |
Charcot-Marie-Tooth Disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0008325 |
BXGD000529 |
Cholecystitis |
Digestive System Diseases |
| C0008350 |
BXGD000531 |
Cholelithiasis |
Digestive System Diseases |
| C0008489 |
BXGD000546 |
Chorea |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0009319 |
BXGD000596 |
Colitis |
Digestive System Diseases |
| C0009324 |
BXGD000597 |
Ulcerative Colitis |
Digestive System Diseases |
| C0009402 |
BXGD000605 |
Colorectal Carcinoma |
Digestive System Diseases; Neoplasms |
| C0010054 |
BXGD000647 |
Coronary Arteriosclerosis |
Cardiovascular Diseases |
| C0010068 |
BXGD000648 |
Coronary heart disease |
Cardiovascular Diseases |
| C0010278 |
BXGD000660 |
Craniosynostosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0010346 |
BXGD000664 |
Crohn Disease |
Digestive System Diseases |
| C0010709 |
BXGD000689 |
Cyst |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0011103 |
BXGD000697 |
Decerebrate State |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0011168 |
BXGD000700 |
Deglutition Disorders |
Digestive System Diseases; Otorhinolaryngologic Diseases |
| C0011253 |
BXGD000706 |
Delusions |
Behavior and Behavior Mechanisms |
| C0011265 |
BXGD000708 |
Presenile dementia |
Nervous System Diseases; Mental Disorders |
| C0011269 |
BXGD000710 |
Dementia, Vascular |
Nervous System Diseases; Mental Disorders; Cardiovascular Diseases |
| C0011303 |
BXGD000712 |
Demyelinating Diseases |
Nervous System Diseases |
| C0011570 |
BXGD000729 |
Mental Depression |
Behavior and Behavior Mechanisms |
| C0011581 |
BXGD000733 |
Depressive disorder |
Mental Disorders |
| 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 |
| C0012236 |
BXGD000772 |
DiGeorge Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases |
| C0012813 |
BXGD000791 |
Diverticulitis |
Digestive System Diseases |
| C0013080 |
BXGD000797 |
Down Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0013362 |
BXGD000817 |
Dysarthria |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0013421 |
BXGD000837 |
Dystonia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0014038 |
BXGD000878 |
Encephalitis |
Nervous System Diseases |
| C0014070 |
BXGD000887 |
Encephalomyelitis |
Infections; Nervous System Diseases |
| C0014544 |
BXGD000926 |
Epilepsy |
Nervous System Diseases |
| C0014550 |
BXGD000930 |
Myoclonic Epilepsy |
Nervous System Diseases |
| C0014859 |
BXGD000961 |
Esophageal Neoplasms |
Digestive System Diseases; Neoplasms |
| C0014868 |
BXGD000965 |
Esophagitis |
Digestive System Diseases |
| C0015732 |
BXGD001018 |
Fecal Incontinence |
Digestive System Diseases |
| C0015967 |
BXGD001030 |
Fever |
Pathological Conditions, Signs and Symptoms |
| C0016978 |
BXGD001087 |
gallbladder neoplasm |
Digestive System Diseases; Neoplasms |
| C0017205 |
BXGD001105 |
Gaucher Disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0017636 |
BXGD001131 |
Glioblastoma |
Neoplasms |
| C0018524 |
BXGD001200 |
Hallucinations |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms |
| C0018790 |
BXGD001221 |
Cardiac Arrest |
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 |
| C0019163 |
BXGD001295 |
Hepatitis B |
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 |
| C0019270 |
BXGD001311 |
Hernia |
Pathological Conditions, Signs and Symptoms |
| C0019294 |
BXGD001314 |
Hernia, Inguinal |
Pathological Conditions, Signs and Symptoms |
| C0019360 |
BXGD001327 |
Herpes zoster disease |
Infections |
| C0020456 |
BXGD001392 |
Hyperglycemia |
Nutritional and Metabolic Diseases |
| C0020473 |
BXGD001396 |
Hyperlipidemia |
Nutritional and Metabolic Diseases |
| C0020538 |
BXGD001422 |
Hypertensive disease |
Cardiovascular Diseases |
| C0020676 |
BXGD001462 |
Hypothyroidism |
Endocrine System Diseases |
| C0020757 |
BXGD001466 |
Ichthyoses |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases |
| C0020758 |
BXGD001467 |
Congenital ichthyosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases |
| C0021051 |
BXGD001475 |
Immunologic Deficiency Syndromes |
Immune System Diseases |
| C0021167 |
BXGD001487 |
Incontinence |
Nervous System Diseases |
| C0021390 |
BXGD001503 |
Inflammatory Bowel Diseases |
Digestive System Diseases |
| C0022104 |
BXGD001529 |
Irritable Bowel Syndrome |
Digestive System Diseases |
| C0022568 |
BXGD001552 |
Keratitis |
Eye 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 |
| C0022672 |
BXGD001574 |
Acute Kidney Tubular Necrosis |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0023520 |
BXGD001678 |
Leukodystrophy |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0023521 |
BXGD001679 |
Globoid cell leukodystrophy |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0023522 |
BXGD001680 |
Leukodystrophy, Metachromatic |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0024115 |
BXGD001732 |
Lung diseases |
Respiratory Tract Diseases |
| C0024117 |
BXGD001734 |
Chronic Obstructive Airway Disease |
Respiratory Tract Diseases |
| C0024141 |
BXGD001740 |
Lupus Erythematosus, Systemic |
Skin and Connective Tissue Diseases; Immune System Diseases |
| C0025064 |
BXGD001825 |
Mediastinitis |
Respiratory Tract Diseases |
| C0025517 |
BXGD001875 |
Metabolic Diseases |
Nutritional and Metabolic Diseases |
| C0026709 |
BXGD001924 |
Mucopolysaccharidosis VI |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases |
| C0026769 |
BXGD001930 |
Multiple Sclerosis |
Immune System Diseases; Nervous System Diseases |
| C0026827 |
BXGD001936 |
Muscle hypotonia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0026838 |
BXGD001938 |
Muscle Spasticity |
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases |
| C0027051 |
BXGD001963 |
Myocardial Infarction |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0027430 |
BXGD001988 |
Nasal Polyps |
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Otorhinolaryngologic Diseases |
| C0027627 |
BXGD002006 |
Neoplasm Metastasis |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0027651 |
BXGD002009 |
Neoplasms |
Neoplasms |
| C0027765 |
BXGD002033 |
nervous system disorder |
Nervous System Diseases |
| C0027809 |
BXGD002040 |
Neurilemmoma |
Neoplasms |
| C0027819 |
BXGD002043 |
Neuroblastoma |
Neoplasms |
| C0028259 |
BXGD002073 |
Nodule |
|
| C0028754 |
BXGD002082 |
Obesity |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases |
| C0029124 |
BXGD002113 |
Optic Atrophy |
Eye Diseases; Nervous System Diseases |
| C0029408 |
BXGD002137 |
Degenerative polyarthritis |
Musculoskeletal Diseases |
| C0029410 |
BXGD002138 |
Osteoarthritis of hip |
Musculoskeletal Diseases |
| C0029454 |
BXGD002155 |
Osteopetrosis |
Musculoskeletal Diseases |
| C0029456 |
BXGD002157 |
Osteoporosis |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C0030193 |
BXGD002191 |
Pain |
Pathological Conditions, Signs and Symptoms |
| C0030201 |
BXGD002194 |
Pain, Postoperative |
Pathological Conditions, Signs and Symptoms |
| C0030524 |
BXGD002236 |
Paratuberculosis |
Infections; Animal Diseases |
| C0030567 |
BXGD002240 |
Parkinson Disease |
Nervous System Diseases |
| C0031117 |
BXGD002285 |
Peripheral Neuropathy |
Nervous System Diseases |
| C0032584 |
BXGD002363 |
polyps |
Pathological Conditions, Signs and Symptoms |
| C0032897 |
BXGD002378 |
Prader-Willi Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0033036 |
BXGD002389 |
Atrial Premature Complexes |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0033626 |
BXGD002412 |
Protein Deficiency |
Nutritional and Metabolic Diseases |
| C0034372 |
BXGD002480 |
Quadriplegia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0034935 |
BXGD002497 |
Babinski Reflex |
|
| C0036161 |
BXGD002580 |
Sandhoff Disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0036337 |
BXGD002598 |
Schizoaffective Disorder |
Mental Disorders |
| C0036341 |
BXGD002600 |
Schizophrenia |
Mental Disorders |
| C0036572 |
BXGD002625 |
Seizures |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0036690 |
BXGD002632 |
Septicemia |
Pathological Conditions, Signs and Symptoms; Infections |
| C0037384 |
BXGD002693 |
Snoring |
Pathological Conditions, Signs and Symptoms |
| C0037899 |
BXGD002710 |
Sphingolipidoses |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0037930 |
BXGD002714 |
Spinal Cord Neoplasms |
Neoplasms; Nervous System Diseases |
| C0037939 |
BXGD002716 |
Spinal Neoplasms |
Neoplasms; Musculoskeletal Diseases |
| C0038013 |
BXGD002725 |
Ankylosing spondylitis |
Musculoskeletal Diseases |
| C0038454 |
BXGD002760 |
Cerebrovascular accident |
Nervous System Diseases; Cardiovascular Diseases |
| C0039373 |
BXGD002809 |
Tay-Sachs Disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0040028 |
BXGD002835 |
Thrombocythemia, Essential |
Hemic and Lymphatic Diseases |
| C0040136 |
BXGD002845 |
Thyroid Neoplasm |
Neoplasms; Endocrine System Diseases |
| C0041296 |
BXGD002903 |
Tuberculosis |
Infections |
| C0041696 |
BXGD002932 |
Unipolar Depression |
Mental Disorders |
| C0041974 |
BXGD002945 |
Urethral Stenosis |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0042024 |
BXGD002949 |
Urinary Incontinence |
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0042025 |
BXGD002950 |
Urinary Stress Incontinence |
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0042109 |
BXGD002957 |
Urticaria |
Skin and Connective Tissue Diseases; Immune System Diseases |
| C0079588 |
BXGD003084 |
Ichthyosis, X-Linked |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases |
| C0080178 |
BXGD003107 |
Spina Bifida |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0085078 |
BXGD003118 |
Lysosomal Storage Diseases |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0085131 |
BXGD003129 |
Gangliosidosis GM1 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0085633 |
BXGD003216 |
Mood swings |
Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0086543 |
BXGD003294 |
Cataract |
Eye Diseases |
| C0151786 |
BXGD003475 |
Muscle Weakness |
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases |
| C0151888 |
BXGD003497 |
Hyporeflexia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0151889 |
BXGD003498 |
Hyperreflexia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0152018 |
BXGD003518 |
Esophageal carcinoma |
Digestive System Diseases; Neoplasms |
| C0152021 |
BXGD003520 |
Congenital heart disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C0152025 |
BXGD003521 |
Polyneuropathy |
Nervous System Diseases |
| C0153676 |
BXGD003679 |
Secondary malignant neoplasm of lung |
Neoplasms; Respiratory Tract Diseases |
| C0162565 |
BXGD003957 |
Acute intermittent porphyria |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases |
| C0162770 |
BXGD003980 |
Right Ventricular Hypertrophy |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0162871 |
BXGD003996 |
Aortic Aneurysm, Abdominal |
Cardiovascular Diseases |
| C0175754 |
BXGD004015 |
Agenesis of corpus callosum |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0178874 |
BXGD004037 |
Tumor Progression |
Pathological Conditions, Signs and Symptoms |
| C0205699 |
BXGD004110 |
Carcinomatosis |
Neoplasms |
| C0220704 |
BXGD004327 |
Shprintzen syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases |
| C0220710 |
BXGD004329 |
Medium-chain acyl-coenzyme A dehydrogenase deficiency |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0221069 |
BXGD004387 |
Anterior Spinal Artery Syndrome |
Nervous System Diseases; Cardiovascular Diseases |
| C0221106 |
BXGD004390 |
Alkalemia |
|
| C0221505 |
BXGD004466 |
Lesion of brain |
|
| C0221764 |
BXGD004476 |
Chronic psychosis |
Pathological Conditions, Signs and Symptoms; Mental Disorders |
| C0232197 |
BXGD004536 |
Fibrillation |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0232769 |
BXGD004563 |
Abnormal gallbladder function |
|
| C0233514 |
BXGD004584 |
Abnormal behavior |
Behavior and Behavior Mechanisms |
| C0233794 |
BXGD004618 |
Memory impairment |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms |
| C0233844 |
BXGD004620 |
Clumsiness |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders |
| C0234376 |
BXGD004659 |
Action Tremor |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0234632 |
BXGD004691 |
Reduced visual acuity |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C0234985 |
BXGD004708 |
Mental deterioration |
Mental Disorders |
| C0235031 |
BXGD004714 |
Neurologic Symptoms |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0239981 |
BXGD005011 |
Hypoalbuminemia |
Hemic and Lymphatic Diseases |
| C0240066 |
BXGD005016 |
Iron deficiency |
Nutritional and Metabolic Diseases |
| C0240602 |
BXGD005046 |
opioid use |
|
| C0241910 |
BXGD005123 |
Autoimmune Chronic Hepatitis |
Digestive System Diseases; Immune System Diseases |
| C0242339 |
BXGD005150 |
Dyslipidemias |
Nutritional and Metabolic Diseases |
| C0242379 |
BXGD005157 |
Malignant neoplasm of lung |
Neoplasms; Respiratory Tract Diseases |
| C0242510 |
BXGD005173 |
Drug usage |
Chemically-Induced Disorders; Mental Disorders |
| C0243026 |
BXGD005210 |
Sepsis |
Pathological Conditions, Signs and Symptoms; Infections |
| C0262630 |
BXGD005262 |
Reduced concentration span |
Behavior and Behavior Mechanisms |
| C0265101 |
BXGD005454 |
Carotid artery occlusion |
Nervous System Diseases; Cardiovascular Diseases |
| C0268263 |
BXGD005873 |
Multiple Sulfatase Deficiency Disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0268547 |
BXGD005979 |
Argininosuccinic Aciduria |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0270922 |
BXGD006134 |
Peripheral demyelinating neuropathy |
Immune System Diseases; Nervous System Diseases |
| C0277524 |
BXGD006468 |
Infectious colitis |
Digestive System Diseases |
| C0278134 |
BXGD006498 |
Absence of sensation |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0278704 |
BXGD006567 |
Malignant Childhood Neoplasm |
Neoplasms |
| C0278883 |
BXGD006614 |
Metastatic melanoma |
Neoplasms |
| C0279583 |
BXGD006640 |
Childhood T Acute Lymphoblastic Leukemia |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0279592 |
BXGD006643 |
Adult T Acute Lymphoblastic Leukemia |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0281361 |
BXGD006774 |
Adenocarcinoma of pancreas |
Digestive System Diseases; Neoplasms; Endocrine System Diseases |
| C0282160 |
BXGD006797 |
Aplasia Cutis Congenita |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases |
| C0282492 |
BXGD006805 |
Sneddon Syndrome |
Skin and Connective Tissue Diseases; Nervous System Diseases; Cardiovascular Diseases |
| C0311394 |
BXGD006884 |
Difficulty walking |
Pathological Conditions, Signs and Symptoms |
| C0332853 |
BXGD006901 |
Anastomosis |
|
| C0334108 |
BXGD006994 |
Multiple polyps |
Pathological Conditions, Signs and Symptoms |
| C0338106 |
BXGD007167 |
Adenocarcinoma of colon |
Digestive System Diseases; Neoplasms |
| C0338656 |
BXGD007211 |
Impaired cognition |
Mental Disorders |
| C0344315 |
BXGD007666 |
Depressed mood |
Behavior and Behavior Mechanisms |
| C0345905 |
BXGD007746 |
Intrahepatic Cholangiocarcinoma |
Neoplasms |
| C0346957 |
BXGD007836 |
Disseminated Malignant Neoplasm |
Neoplasms |
| C0392322 |
BXGD008037 |
Undifferentiated schizophrenia |
Mental Disorders |
| C0401067 |
BXGD008271 |
Unilateral inguinal hernia NOS |
Pathological Conditions, Signs and Symptoms |
| C0403447 |
BXGD008285 |
Chronic Kidney Insufficiency |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0426970 |
BXGD008598 |
Spastic Quadriplegia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0427144 |
BXGD008607 |
Toe-walking gait |
|
| C0429028 |
BXGD008646 |
QT interval feature (observable entity) |
|
| C0452138 |
BXGD008831 |
Sensorineural hearing loss, bilateral |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases |
| C0497327 |
BXGD009061 |
Dementia |
Nervous System Diseases; Mental Disorders |
| C0520559 |
BXGD009091 |
Numbness of tongue |
Stomatognathic Diseases |
| C0520679 |
BXGD009101 |
Sleep Apnea, Obstructive |
Respiratory Tract Diseases; Nervous System Diseases |
| C0522214 |
BXGD009196 |
Abnormal visual evoked potential |
Nervous System Diseases |
| C0524620 |
BXGD009236 |
Metabolic Syndrome X |
Nutritional and Metabolic Diseases |
| C0524851 |
BXGD009246 |
Neurodegenerative Disorders |
Nervous System Diseases |
| C0542223 |
BXGD009274 |
Loss of speech |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0542476 |
BXGD009276 |
Forgetful |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0543699 |
BXGD009293 |
ASA intolerant asthma |
Respiratory Tract Diseases; Immune System Diseases |
| C0546837 |
BXGD009343 |
Malignant neoplasm of esophagus |
Digestive System Diseases; Neoplasms |
| C0549473 |
BXGD009384 |
Thyroid carcinoma |
Neoplasms; Endocrine System Diseases |
| C0563625 |
BXGD009484 |
Agnosia for Pain |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms |
| C0566602 |
BXGD009489 |
Primary sclerosing cholangitis |
Digestive System Diseases |
| C0575081 |
BXGD009512 |
Gait abnormality |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0577631 |
BXGD009535 |
Carotid Atherosclerosis |
Nervous System Diseases; Cardiovascular Diseases |
| C0578870 |
BXGD009553 |
Chronic idiopathic urticaria |
Skin and Connective Tissue Diseases; Immune System Diseases |
| C0596263 |
BXGD009639 |
Carcinogenesis |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0678222 |
BXGD009749 |
Breast Carcinoma |
Neoplasms; Skin and Connective Tissue Diseases |
| C0684249 |
BXGD009790 |
Carcinoma of lung |
Neoplasms; Respiratory Tract Diseases |
| C0699790 |
BXGD009866 |
Colon Carcinoma |
Digestive System Diseases; Neoplasms |
| C0700095 |
BXGD009875 |
Central neuroblastoma |
Neoplasms; Nervous System Diseases |
| C0740406 |
BXGD009992 |
Incarcerated hernia |
Pathological Conditions, Signs and Symptoms |
| C0741923 |
BXGD010045 |
cardiac event |
|
| C0742343 |
BXGD010061 |
Acute Chest Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Hemic and Lymphatic Diseases |
| C0746102 |
BXGD010136 |
Chronic lung disease |
Respiratory Tract Diseases |
| C0751276 |
BXGD010374 |
Metachromatic leukodystrophy, juvenile type |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0751278 |
BXGD010375 |
Metachromatic Leukodystrophy, Infant |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0751279 |
BXGD010376 |
Metachromatic Leukodystrophy, Adult-Type (disorder) |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0751651 |
BXGD010539 |
Mitochondrial Diseases |
Nutritional and Metabolic Diseases |
| C0751778 |
BXGD010587 |
Myoclonic Epilepsies, Progressive |
Nervous System Diseases |
| C0751785 |
BXGD010594 |
Unverricht-Lundborg Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0751870 |
BXGD010622 |
Heredodegenerative Disorders, Nervous System |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0796466 |
BXGD010833 |
Refractory cytopenia with multilineage dysplasia |
Hemic and Lymphatic Diseases |
| C0812413 |
BXGD010847 |
Malignant Pleural Mesothelioma |
Neoplasms; Respiratory Tract Diseases |
| C0850666 |
BXGD010901 |
Infection caused by Helicobacter pylori |
Infections |
| C0850703 |
BXGD010905 |
Frequent falls |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0852949 |
BXGD010957 |
Arteriopathic disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0860603 |
BXGD011236 |
Anxiety symptoms |
|
| C0868908 |
BXGD011302 |
Pancolitis |
Digestive System Diseases |
| C0872084 |
BXGD011319 |
Sarcopenia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0878575 |
BXGD011372 |
Peripheral demyelination |
Nervous System Diseases |
| C0917808 |
BXGD011415 |
Vegetative State |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0920253 |
BXGD011461 |
Emergence Delirium |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0936282 |
BXGD011487 |
Blastoma |
Neoplasms |
| C0948008 |
BXGD011499 |
Ischemic stroke |
Nervous System Diseases; Cardiovascular Diseases |
| C0948089 |
BXGD011504 |
Acute Coronary Syndrome |
Cardiovascular Diseases |
| C0948163 |
BXGD011511 |
Leukoaraiosis |
Pathological Conditions, Signs and Symptoms |
| C0948268 |
BXGD011523 |
Hemodynamic instability |
|
| C1145670 |
BXGD011764 |
Respiratory Failure |
Respiratory Tract Diseases |
| C1263726 |
BXGD011891 |
Sulfatiduria |
|
| C1269683 |
BXGD012001 |
Major Depressive Disorder |
Mental Disorders |
| C1269955 |
BXGD012005 |
Tumor Cell Invasion |
|
| C1279945 |
BXGD012124 |
Acute interstitial pneumonia |
Respiratory Tract Diseases |
| C1297882 |
BXGD012244 |
Partial Trisomy |
Pathological Conditions, Signs and Symptoms |
| C1306459 |
BXGD012361 |
Primary malignant neoplasm |
Neoplasms |
| C1306460 |
BXGD012362 |
Primary malignant neoplasm of lung |
Neoplasms; Respiratory Tract Diseases |
| C1321551 |
BXGD012436 |
Shprintzen-Goldberg syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases |
| C1328500 |
BXGD012468 |
Intraoperative hypertension |
|
| C1333990 |
BXGD012670 |
Hereditary Nonpolyposis Colorectal Cancer |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Nutritional and Metabolic Diseases |
| C1335302 |
BXGD012775 |
Pancreatic Ductal Adenocarcinoma |
Digestive System Diseases; Neoplasms; Endocrine System Diseases |
| C1412000 |
BXGD013049 |
Mesenteric vascular insufficiency |
Digestive System Diseases; Cardiovascular Diseases |
| C1510475 |
BXGD013171 |
Diverticulosis |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C1510586 |
BXGD013176 |
Autism Spectrum Disorders |
Mental Disorders |
| C1527390 |
BXGD013285 |
Neoplasms, Intracranial |
Neoplasms; Nervous System Diseases |
| 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 |
| C1565489 |
BXGD013401 |
Renal Insufficiency |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C1608408 |
BXGD013434 |
Malignant transformation |
|
| C1621958 |
BXGD013468 |
Glioblastoma Multiforme |
Neoplasms |
| C1704436 |
BXGD013564 |
Peripheral Arterial Diseases |
Cardiovascular Diseases |
| C1706192 |
BXGD013570 |
Sulfatidosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C1720864 |
BXGD013693 |
Sulfatidosis, Juvenile, Austin Type |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C1806780 |
BXGD013759 |
Increased CSF protein |
|
| C1832661 |
BXGD013866 |
ANOPHTHALMIA AND PULMONARY HYPOPLASIA |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Respiratory Tract Diseases |
| C1836830 |
BXGD014165 |
Developmental regression |
Mental Disorders |
| C1843885 |
BXGD014616 |
Progressive gait ataxia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C1848916 |
BXGD014985 |
Tay-Sachs Disease, Variant B1 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C1853490 |
BXGD015341 |
22q13.3 Deletion Syndrome |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C1855255 |
BXGD015479 |
Pseudoarylsulfatase A Deficiency |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C1856507 |
BXGD015614 |
Bulbar signs |
|
| C1856565 |
BXGD015618 |
Progressive psychomotor deterioration |
|
| C1857640 |
BXGD015726 |
Decreased nerve conduction velocity |
|
| C1858120 |
BXGD015774 |
Generalized hypotonia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C1859178 |
BXGD015859 |
Progressive peripheral neuropathy |
|
| C1859736 |
BXGD015929 |
Progressive spastic quadriplegia |
|
| C1868263 |
BXGD016495 |
Platelet Aggregation, Spontaneous |
Hemic and Lymphatic Diseases |
| C1868528 |
BXGD016503 |
Orthostatic hypotension due to autonomic dysfunction |
Nervous System Diseases; Cardiovascular Diseases |
| C1956346 |
BXGD016627 |
Coronary Artery Disease |
Cardiovascular Diseases |
| C1961099 |
BXGD016672 |
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C1963167 |
BXGD016686 |
Memory Impairment, CTCAE 3.0 |
|
| 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 |
| C2363129 |
BXGD017095 |
Benign Rolandic Epilepsy |
Nervous System Diseases |
| C2674608 |
BXGD017250 |
Feeding difficulties in infancy |
|
| C2713319 |
BXGD017493 |
Arylsulfatase A Deficiency |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C2826323 |
BXGD017790 |
Refractory Cytopenia of Childhood |
|
| C2919796 |
BXGD017880 |
Glycogen storage disease type Ia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C2919828 |
BXGD017881 |
Chronic ulcerative colitis |
Digestive System Diseases |
| C2931822 |
BXGD018068 |
Nasopharyngeal carcinoma |
Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases |
| C2937222 |
BXGD018155 |
Chronic ulcerative proctitis |
Digestive System Diseases |
| C2938924 |
BXGD018167 |
Oestrogen receptor positive breast cancer |
|
| C2939419 |
BXGD018178 |
Secondary Neoplasm |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C3160718 |
BXGD018468 |
PARKINSON DISEASE, LATE-ONSET |
|
| C3163918 |
BXGD018520 |
Tumor thrombus |
Cardiovascular Diseases |
| C3203102 |
BXGD018555 |
Idiopathic pulmonary arterial hypertension |
Respiratory Tract Diseases |
| C3273225 |
BXGD018648 |
Hereditary Neurodegenerative Disorder |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C3278509 |
BXGD018742 |
Spinal fusion |
|
| C3539878 |
BXGD019087 |
Triple Negative Breast Neoplasms |
Neoplasms; Skin and Connective Tissue Diseases |
| C3662272 |
BXGD019269 |
Drug pseudoallergy |
|
| C3697716 |
BXGD019359 |
Acute flaccid paralysis |
|
| 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 |
| C3845502 |
BXGD019809 |
Myocardial infarction, stroke |
|
| C3853540 |
BXGD019820 |
Aspirin exacerbated respiratory disease |
Pathological Conditions, Signs and Symptoms; Infections; Respiratory Tract Diseases; Immune System Diseases; Chemically-Induced Disorders; Otorhinolaryngologic Diseases |
| C3887662 |
BXGD019914 |
Intraspinal Neoplasm |
Neoplasms; Musculoskeletal Diseases; Nervous System Diseases |
| C3887938 |
BXGD019929 |
Deuteranomaly |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C3888970 |
BXGD019997 |
Embolic stroke of undetermined source |
|
| C4017091 |
BXGD020401 |
ARYLSULFATASE A PSEUDODEFICIENCY |
|
| C4017093 |
BXGD020402 |
METACHROMATIC LEUKODYSTROPHY, LATE-ONSET |
|
| C4017094 |
BXGD020403 |
METACHROMATIC LEUKODYSTROPHY, SEVERE |
|
| C4017095 |
BXGD020404 |
ARYLSULFATASE A PSEUDODEFICIENCY, SEVERE |
|
| C4017096 |
BXGD020405 |
ARYLSULFATASE A PSEUDODEFICIENCY, INTERMEDIATE |
|
| C4017847 |
BXGD020459 |
METACHROMATIC LEUKODYSTROPHY, MILD |
|
| C4021087 |
BXGD020546 |
Abnormal social behavior |
Behavior and Behavior Mechanisms |
| C4021727 |
BXGD020736 |
EMG: neuropathic changes |
|
| C4021768 |
BXGD020766 |
Abnormality of metabolism/homeostasis |
|
| C4022658 |
BXGD020945 |
Punctate periventricular T2 hyperintense foci |
|
| C4024961 |
BXGD021503 |
Metachromatic leukodystrophy variant |
|
| C4025272 |
BXGD021615 |
Peripheral arterial stenosis |
|
| C4025350 |
BXGD021650 |
Abnormality of glycosphingolipid metabolism |
|
| C4025614 |
BXGD021695 |
EMG: chronic denervation signs |
|
| C4045991 |
BXGD021888 |
Perihilar Cholangiocarcinoma |
Neoplasms |
| C4049381 |
BXGD021928 |
Cancer-associated thrombosis |
|
| C4050504 |
BXGD021963 |
Ectomesenchymal Chondromyxoid Tumor |
|
| C4082299 |
BXGD022088 |
Bulbar palsy |
Nervous System Diseases |
| C4086165 |
BXGD022126 |
Childhood Neuroblastoma |
Neoplasms |
| C4255010 |
BXGD022310 |
Non-ST Elevated Myocardial Infarction |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C4284013 |
BXGD022428 |
Primary cholangiocarcinoma of intrahepatic biliary tract |
Neoplasms |
| C4285807 |
BXGD022455 |
Behavioral and psychological symptoms of dementia |
|
| C4288891 |
BXGD022486 |
Infant T Acute Lymphoblastic Leukemia |
|
| C4290140 |
BXGD022508 |
recurrent myocardial infarction |
|
| C4521042 |
BXGD023055 |
Complete Trisomy 21 Syndrome |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C4551691 |
BXGD023394 |
Urethral stricture |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C4551915 |
BXGD023441 |
Gait Disturbance, CTCAE |
|
| C4553743 |
BXGD023548 |
Spasticity, CTCAE |
|
| C4553765 |
BXGD023551 |
Memory Impairment, CTCAE 5.0 |
|
| C4721453 |
BXGD023744 |
Peripheral Nervous System Diseases |
Nervous System Diseases |
| C4721555 |
BXGD023755 |
Autoimmune hepatitis |
Digestive System Diseases |
| C4721772 |
BXGD023767 |
Postoperative delirium |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C4722085 |
BXGD023788 |
Malignant neoplasm of colon and/or rectum |
|
| C4722518 |
BXGD023806 |
Triple-Negative Breast Carcinoma |
Neoplasms; Skin and Connective Tissue Diseases |
| C4733092 |
BXGD023907 |
estrogen receptor-negative breast cancer |
|