| C0002726 |
BXGD000125 |
Amyloidosis |
Nutritional and Metabolic Diseases |
| C0002736 |
BXGD000127 |
Amyotrophic Lateral Sclerosis |
Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0002871 |
BXGD000132 |
Anemia |
Hemic and Lymphatic Diseases |
| C0002880 |
BXGD000139 |
Autoimmune hemolytic anemia |
Immune System Diseases; Hemic and Lymphatic Diseases |
| C0003850 |
BXGD000225 |
Arteriosclerosis |
Cardiovascular Diseases |
| C0003886 |
BXGD000238 |
Arthrogryposis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0004096 |
BXGD000252 |
Asthma |
Respiratory Tract Diseases; Immune System Diseases |
| C0004114 |
BXGD000255 |
Astrocytoma |
Neoplasms |
| C0004153 |
BXGD000260 |
Atherosclerosis |
Cardiovascular Diseases |
| C0005684 |
BXGD000319 |
Malignant neoplasm of urinary bladder |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0005859 |
BXGD000342 |
Bloom Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases |
| C0006118 |
BXGD000372 |
Brain Neoplasms |
Neoplasms; Nervous System Diseases |
| C0006142 |
BXGD000374 |
Malignant neoplasm of breast |
Neoplasms; Skin and Connective Tissue Diseases |
| C0006309 |
BXGD000392 |
Brucellosis |
Infections |
| C0006826 |
BXGD000408 |
Malignant Neoplasms |
Neoplasms |
| C0007097 |
BXGD000424 |
Carcinoma |
Neoplasms |
| 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 |
| C0007847 |
BXGD000492 |
Malignant tumor of cervix |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications |
| C0007959 |
BXGD000507 |
Charcot-Marie-Tooth Disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0008533 |
BXGD000556 |
Hemophilia B |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0009081 |
BXGD000581 |
Congenital clubfoot |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0009917 |
BXGD000635 |
Contracture |
Musculoskeletal Diseases |
| C0010200 |
BXGD000653 |
Coughing |
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases |
| C0010278 |
BXGD000660 |
Craniosynostosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0010403 |
BXGD000668 |
Cryoglobulinemia |
Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases |
| C0011881 |
BXGD000760 |
Diabetic Nephropathy |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases |
| C0013264 |
BXGD000808 |
Muscular Dystrophy, Duchenne |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases |
| C0013363 |
BXGD000818 |
Dysautonomia |
Nervous System Diseases |
| C0014009 |
BXGD000876 |
Empyema |
Pathological Conditions, Signs and Symptoms; Infections |
| C0014060 |
BXGD000882 |
Encephalitis, St. Louis |
Infections; Nervous System Diseases |
| C0014474 |
BXGD000917 |
Ependymoma |
Neoplasms |
| C0014550 |
BXGD000930 |
Myoclonic Epilepsy |
Nervous System Diseases |
| C0015230 |
BXGD000969 |
Exanthema |
Skin and Connective Tissue Diseases |
| C0015826 |
BXGD001022 |
Fenestration (morphologic abnormality) |
|
| C0016065 |
BXGD001046 |
Polyostotic fibrous dysplasia |
Musculoskeletal Diseases |
| C0016506 |
BXGD001062 |
Foot Deformities |
Musculoskeletal Diseases |
| C0017411 |
BXGD001108 |
Female Genital Diseases |
Female Urogenital Diseases and Pregnancy Complications |
| C0017636 |
BXGD001131 |
Glioblastoma |
Neoplasms |
| C0017638 |
BXGD001132 |
Glioma |
Neoplasms |
| C0017661 |
BXGD001139 |
IGA Glomerulonephritis |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases |
| C0017665 |
BXGD001141 |
Membranous glomerulonephritis |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases |
| C0018798 |
BXGD001223 |
Congenital Heart Defects |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C0018816 |
BXGD001234 |
Heart 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 |
| C0019158 |
BXGD001293 |
Hepatitis |
Digestive System Diseases |
| C0019159 |
BXGD001294 |
Hepatitis A |
Digestive System Diseases; Infections |
| C0019196 |
BXGD001301 |
Hepatitis C |
Digestive System Diseases; Infections |
| C0019562 |
BXGD001336 |
Von Hippel-Lindau Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases |
| C0020456 |
BXGD001392 |
Hyperglycemia |
Nutritional and Metabolic Diseases |
| C0020538 |
BXGD001422 |
Hypertensive disease |
Cardiovascular Diseases |
| C0021364 |
BXGD001500 |
Male infertility |
Male Urogenital Diseases |
| C0022346 |
BXGD001537 |
Icterus |
Pathological Conditions, Signs and Symptoms |
| C0022548 |
BXGD001551 |
Keloid |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases |
| C0022575 |
BXGD001555 |
Keratoconjunctivitis Sicca |
Eye Diseases |
| C0022577 |
BXGD001556 |
Keratoconjunctivitis, Vernal |
Eye Diseases; Immune System Diseases |
| C0023267 |
BXGD001626 |
Fibroid Tumor |
Neoplasms |
| C0023530 |
BXGD001683 |
Leukopenia |
Hemic and Lymphatic Diseases |
| C0023890 |
BXGD001713 |
Liver Cirrhosis |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C0024117 |
BXGD001734 |
Chronic Obstructive Airway Disease |
Respiratory Tract Diseases |
| C0024141 |
BXGD001740 |
Lupus Erythematosus, Systemic |
Skin and Connective Tissue Diseases; Immune System Diseases |
| C0024535 |
BXGD001785 |
Malaria, Falciparum |
Infections |
| C0024623 |
BXGD001791 |
Malignant neoplasm of stomach |
Digestive System Diseases; Neoplasms |
| C0025149 |
BXGD001826 |
Medulloblastoma |
Neoplasms |
| C0025202 |
BXGD001832 |
melanoma |
Neoplasms |
| C0025958 |
BXGD001882 |
Microcephaly |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases |
| C0026821 |
BXGD001933 |
Muscle Cramp |
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases |
| C0026827 |
BXGD001936 |
Muscle hypotonia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0026847 |
BXGD001940 |
Spinal Muscular Atrophy |
Nervous System Diseases |
| C0026848 |
BXGD001941 |
Myopathy |
Musculoskeletal Diseases; Nervous System Diseases |
| C0026896 |
BXGD001946 |
Myasthenia Gravis |
Neoplasms; Immune System Diseases; Nervous System Diseases |
| C0027051 |
BXGD001963 |
Myocardial Infarction |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0027059 |
BXGD001965 |
Myocarditis |
Cardiovascular Diseases |
| C0027430 |
BXGD001988 |
Nasal Polyps |
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Otorhinolaryngologic Diseases |
| C0027533 |
BXGD001995 |
Neck Neoplasms |
Neoplasms |
| C0027627 |
BXGD002006 |
Neoplasm Metastasis |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0027651 |
BXGD002009 |
Neoplasms |
Neoplasms |
| C0027819 |
BXGD002043 |
Neuroblastoma |
Neoplasms |
| C0027868 |
BXGD002053 |
Neuromuscular Diseases |
Nervous System Diseases |
| C0027947 |
BXGD002061 |
Neutropenia |
Hemic and Lymphatic Diseases |
| C0028968 |
BXGD002103 |
Olivopontocerebellar Atrophies |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0029124 |
BXGD002113 |
Optic Atrophy |
Eye Diseases; Nervous System Diseases |
| C0029172 |
BXGD002120 |
Oral Submucous Fibrosis |
Stomatognathic Diseases |
| C0029408 |
BXGD002137 |
Degenerative polyarthritis |
Musculoskeletal Diseases |
| C0030193 |
BXGD002191 |
Pain |
Pathological Conditions, Signs and Symptoms |
| C0030305 |
BXGD002206 |
Pancreatitis |
Digestive System Diseases |
| C0030552 |
BXGD002238 |
Paresis |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0030567 |
BXGD002240 |
Parkinson Disease |
Nervous System Diseases |
| C0032897 |
BXGD002378 |
Prader-Willi Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0033626 |
BXGD002412 |
Protein Deficiency |
Nutritional and Metabolic Diseases |
| C0033999 |
BXGD002448 |
Pterygium |
Eye Diseases |
| C0034069 |
BXGD002458 |
Pulmonary Fibrosis |
Respiratory Tract Diseases |
| C0035243 |
BXGD002522 |
Respiratory Tract Infections |
Infections; Respiratory Tract Diseases |
| C0036341 |
BXGD002600 |
Schizophrenia |
Mental Disorders |
| C0036421 |
BXGD002613 |
Systemic Scleroderma |
Skin and Connective Tissue Diseases |
| C0036439 |
BXGD002615 |
Scoliosis, unspecified |
Musculoskeletal Diseases |
| C0037299 |
BXGD002685 |
Skin Ulcer |
Skin and Connective Tissue Diseases |
| C0037763 |
BXGD002699 |
Spasm |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0037933 |
BXGD002715 |
Spinal Diseases |
Musculoskeletal Diseases |
| C0038454 |
BXGD002760 |
Cerebrovascular accident |
Nervous System Diseases; Cardiovascular Diseases |
| C0038828 |
BXGD002780 |
Superior Mesenteric Artery Syndrome |
Digestive System Diseases |
| C0039101 |
BXGD002790 |
synovial sarcoma |
Neoplasms |
| C0039685 |
BXGD002825 |
Tetralogy of Fallot |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C0040517 |
BXGD002872 |
Gilles de la Tourette syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders |
| C0041956 |
BXGD002942 |
Ureteral obstruction |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0042133 |
BXGD002960 |
Uterine Fibroids |
Neoplasms |
| C0042384 |
BXGD002979 |
Vasculitis |
Cardiovascular Diseases |
| C0043116 |
BXGD003028 |
HMN (Hereditary Motor Neuropathy) Proximal Type I |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0079731 |
BXGD003087 |
B-Cell Lymphomas |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0085084 |
BXGD003121 |
Motor Neuron Disease |
Nervous System Diseases |
| C0085655 |
BXGD003226 |
Polymyositis |
Musculoskeletal Diseases; Nervous System Diseases |
| C0085696 |
BXGD003244 |
Chronic prostatitis |
Male Urogenital Diseases |
| C0086445 |
BXGD003285 |
Idiopathic Membranous Glomerulonephritis |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases |
| C0149516 |
BXGD003324 |
Chronic sinusitis |
Infections; Respiratory Tract Diseases; Otorhinolaryngologic Diseases |
| C0149521 |
BXGD003328 |
Pancreatitis, Chronic |
Digestive System Diseases |
| C0151514 |
BXGD003429 |
Atrophic condition of skin |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases |
| C0151650 |
BXGD003454 |
Renal fibrosis |
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital 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 |
| C0152101 |
BXGD003540 |
Hypoplastic Left Heart Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C0152109 |
BXGD003542 |
Juvenile Spinal Muscular Atrophy |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0152256 |
BXGD003575 |
Disuse osteoporosis |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C0153676 |
BXGD003679 |
Secondary malignant neoplasm of lung |
Neoplasms; Respiratory Tract Diseases |
| C0155141 |
BXGD003776 |
Acute conjunctivitis |
Eye Diseases |
| C0155626 |
BXGD003806 |
Acute myocardial infarction |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0162810 |
BXGD003982 |
Cicatrix, Hypertrophic |
Pathological Conditions, Signs and Symptoms |
| C0205710 |
BXGD004112 |
Alpers Syndrome (disorder) |
Immune System Diseases; Nervous System Diseases |
| C0205882 |
BXGD004138 |
Infections, Parvovirus |
Infections |
| C0206734 |
BXGD004279 |
Hemangioblastoma |
Neoplasms |
| C0221013 |
BXGD004363 |
Mastocytosis, Systemic |
Neoplasms; Immune System Diseases |
| C0221054 |
BXGD004381 |
Welander Distal Myopathy |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases |
| C0221629 |
BXGD004467 |
Proximal muscle weakness |
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases |
| C0233401 |
BXGD004575 |
Psychiatric symptom |
|
| C0234146 |
BXGD004626 |
Absent reflex |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0235419 |
BXGD004745 |
Hyperuricemic nephropathy |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases |
| C0235974 |
BXGD004796 |
Pancreatic carcinoma |
Digestive System Diseases; Neoplasms; Endocrine System Diseases |
| C0239548 |
BXGD004984 |
Fasciculation, Tongue |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0239842 |
BXGD005001 |
Tremor of hands |
|
| C0239946 |
BXGD005010 |
Fibrosis, Liver |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C0242422 |
BXGD005163 |
Parkinsonian Disorders |
Nervous System Diseases |
| C0242429 |
BXGD005166 |
Sore Throat |
Infections; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases |
| C0242723 |
BXGD005193 |
Parasitemia |
Pathological Conditions, Signs and Symptoms; Infections |
| C0242852 |
BXGD005197 |
Proliferative vitreoretinopathy |
Eye Diseases |
| C0265950 |
BXGD005588 |
Venous malformation |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C0268274 |
BXGD005877 |
Gangliosidoses, GM2 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0268381 |
BXGD005922 |
Primary amyloidosis |
Neoplasms; Nutritional and Metabolic Diseases; Immune System Diseases |
| C0268596 |
BXGD006000 |
Multiple Acyl Coenzyme A Dehydrogenase Deficiency |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0270764 |
BXGD006100 |
Motor Neuron Disease, Lower |
Nervous System Diseases |
| C0270765 |
BXGD006101 |
Myelopathic Muscular Atrophy |
Nervous System Diseases |
| C0270816 |
BXGD006110 |
epilepsy and migraine |
|
| C0270922 |
BXGD006134 |
Peripheral demyelinating neuropathy |
Immune System Diseases; Nervous System Diseases |
| C0270960 |
BXGD006141 |
Congenital myopathy (disorder) |
Musculoskeletal Diseases; Nervous System Diseases |
| C0278510 |
BXGD006526 |
Childhood Medulloblastoma |
Neoplasms |
| C0278660 |
BXGD006555 |
Adult Synovial Sarcoma |
Neoplasms |
| C0278704 |
BXGD006567 |
Malignant Childhood Neoplasm |
Neoplasms |
| C0278874 |
BXGD006605 |
Adult Ependymoma |
Neoplasms |
| C0278876 |
BXGD006607 |
Adult Medulloblastoma |
Neoplasms |
| C0278878 |
BXGD006609 |
Adult Glioblastoma |
Neoplasms |
| C0278996 |
BXGD006621 |
Malignant Head and Neck Neoplasm |
Neoplasms |
| C0279702 |
BXGD006685 |
Conventional (Clear Cell) Renal Cell Carcinoma |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0279982 |
BXGD006702 |
Childhood Synovial Sarcoma |
Neoplasms |
| C0280474 |
BXGD006748 |
Childhood Glioblastoma |
Neoplasms |
| C0302592 |
BXGD006851 |
Cervix carcinoma |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications |
| C0311262 |
BXGD006871 |
Chronic mesenteric ischemia |
Digestive System Diseases; Cardiovascular Diseases |
| C0332878 |
BXGD006904 |
Congenital contracture |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0333641 |
BXGD006961 |
Atrophic |
Pathological Conditions, Signs and Symptoms |
| C0334121 |
BXGD006996 |
Inflammatory Myofibroblastic Tumor |
Pathological Conditions, Signs and Symptoms |
| C0339543 |
BXGD007267 |
Epiretinal Membrane |
Eye Diseases |
| C0342782 |
BXGD007549 |
Depletion of mitochondrial DNA |
|
| C0343401 |
BXGD007623 |
MRSA - Methicillin resistant Staphylococcus aureus infection |
Infections |
| C0344460 |
BXGD007674 |
Carcinoma ex pleomorphic adenoma |
Neoplasms; Stomatognathic Diseases |
| C0346647 |
BXGD007832 |
Malignant neoplasm of pancreas |
Digestive System Diseases; Neoplasms; Endocrine System Diseases |
| C0375023 |
BXGD007970 |
Respiratory syncytial virus (RSV) infection in conditions classified elsewhere and of unspecified site |
|
| C0376358 |
BXGD007992 |
Malignant neoplasm of prostate |
Neoplasms; Male Urogenital Diseases |
| C0393538 |
BXGD008083 |
Muscular Atrophy, Spinal, Type II |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0393541 |
BXGD008084 |
Distal Spinal Muscular Atrophy |
Nervous System Diseases |
| C0393546 |
BXGD008085 |
Oculopharyngeal Spinal Muscular Atrophy |
Nervous System Diseases |
| C0393547 |
BXGD008086 |
Bulbospinal Neuronopathy |
Nervous System Diseases |
| C0399440 |
BXGD008244 |
Hereditary gingival fibromatosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic 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 |
| C0410158 |
BXGD008408 |
Muscle damage |
|
| C0442874 |
BXGD008814 |
Neuropathy |
Nervous System Diseases |
| C0454455 |
BXGD008835 |
Mirror movements disorder |
Nervous System Diseases |
| C0476273 |
BXGD008986 |
Respiratory distress |
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases |
| C0476403 |
BXGD008992 |
Electromyogram abnormal |
|
| C0520680 |
BXGD009102 |
Sleep Apnea, Central |
Respiratory Tract Diseases; Nervous System Diseases |
| C0521158 |
BXGD009130 |
Recurrent tumor |
|
| C0521607 |
BXGD009146 |
Peritoneal Fibrosis |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C0524851 |
BXGD009246 |
Neurodegenerative Disorders |
Nervous System Diseases |
| C0553580 |
BXGD009399 |
Ewings sarcoma |
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 |
| C0677886 |
BXGD009734 |
Epithelial ovarian cancer |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C0678222 |
BXGD009749 |
Breast Carcinoma |
Neoplasms; Skin and Connective Tissue Diseases |
| C0686619 |
BXGD009835 |
Secondary malignant neoplasm of lymph node |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0699743 |
BXGD009862 |
Congenital muscular dystrophy (disorder) |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases |
| C0699791 |
BXGD009867 |
Stomach Carcinoma |
Digestive System Diseases; Neoplasms |
| C0699885 |
BXGD009869 |
Carcinoma of bladder |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0700095 |
BXGD009875 |
Central neuroblastoma |
Neoplasms; Nervous System Diseases |
| C0700595 |
BXGD009895 |
Spinal Muscular Atrophies of Childhood |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0729233 |
BXGD009922 |
Dissecting aneurysm of the thoracic aorta |
Cardiovascular Diseases |
| C0730328 |
BXGD009959 |
Central Serous Chorioretinopathy |
Eye Diseases |
| C0746674 |
BXGD010147 |
Generalized muscle weakness |
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases |
| C0750403 |
BXGD010235 |
Proximal weakness |
|
| C0751039 |
BXGD010302 |
Cockayne Syndrome, Type I |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases |
| C0751177 |
BXGD010338 |
Cancer of Head |
Neoplasms |
| C0751334 |
BXGD010390 |
Progressive Proximal Myelopathic Muscular Atrophy |
Nervous System Diseases |
| C0751335 |
BXGD010391 |
Scapuloperoneal Form of Spinal Muscular Atrophy |
Nervous System Diseases |
| C0751383 |
BXGD010422 |
Juvenile Neuronal Ceroid Lipofuscinosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0751674 |
BXGD010547 |
Lymphangioleiomyomatosis |
Neoplasms; Immune System Diseases; Hemic and Lymphatic 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 |
| C0751882 |
BXGD010626 |
Myasthenic Syndromes, Congenital |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0796611 |
BXGD010835 |
Newly Diagnosed Childhood Ependymoma |
Neoplasms |
| C0856742 |
BXGD011111 |
Post MI |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0860659 |
BXGD011240 |
Aloof |
|
| C0872084 |
BXGD011319 |
Sarcopenia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0877009 |
BXGD011326 |
Muscle fibrosis |
|
| C0917981 |
BXGD011423 |
Progressive Muscular Atrophy |
Nervous System Diseases |
| C0920350 |
BXGD011466 |
Autoimmune thyroiditis |
Immune System Diseases; Endocrine System Diseases |
| C0948008 |
BXGD011499 |
Ischemic stroke |
Nervous System Diseases; Cardiovascular Diseases |
| C0949445 |
BXGD011575 |
Cervical Dystonia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C1145670 |
BXGD011764 |
Respiratory Failure |
Respiratory Tract Diseases |
| C1263846 |
BXGD011897 |
Attention deficit hyperactivity disorder |
Mental Disorders |
| C1266025 |
BXGD011935 |
Traditional Serrated Adenoma |
Neoplasms |
| C1269955 |
BXGD012005 |
Tumor Cell Invasion |
|
| C1285162 |
BXGD012167 |
Degenerative disorder |
Pathological Conditions, Signs and Symptoms |
| C1301959 |
BXGD012301 |
Bulbar weakness |
Nervous System Diseases |
| C1306459 |
BXGD012361 |
Primary malignant neoplasm |
Neoplasms |
| C1397307 |
BXGD012996 |
Cardiac fibrosis |
|
| C1449647 |
BXGD013089 |
Secondary Peritonitis |
Digestive System Diseases; Infections |
| C1511789 |
BXGD013183 |
Desmoplastic |
|
| C1511934 |
BXGD013184 |
Differentiating Neuroblastoma |
Neoplasms |
| C1512127 |
BXGD013185 |
HER2 gene amplification |
|
| C1514428 |
BXGD013203 |
Primary peritoneal carcinoma |
Digestive System Diseases; Neoplasms |
| C1518715 |
BXGD013226 |
Ovarian Fetiform Teratoma |
|
| C1519670 |
BXGD013241 |
Tumor Angiogenesis |
Pathological Conditions, Signs and Symptoms |
| C1527349 |
BXGD013277 |
Ductal Breast Carcinoma |
Neoplasms |
| C1561643 |
BXGD013363 |
Chronic Kidney Diseases |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C1611743 |
BXGD013456 |
Familial (FPAH) |
|
| C1621958 |
BXGD013468 |
Glioblastoma Multiforme |
Neoplasms |
| C1623038 |
BXGD013475 |
Cirrhosis |
Pathological Conditions, Signs and Symptoms |
| C1658953 |
BXGD013486 |
tumor vasculature |
|
| C1708751 |
BXGD013610 |
Low grade myofibroblastic sarcoma |
|
| C1800706 |
BXGD013755 |
Idiopathic Pulmonary Fibrosis |
Respiratory Tract Diseases |
| C1832661 |
BXGD013866 |
ANOPHTHALMIA AND PULMONARY HYPOPLASIA |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Respiratory Tract Diseases |
| C1838230 |
BXGD014303 |
SPINAL MUSCULAR ATROPHY, TYPE IV |
Nervous System Diseases |
| C1839454 |
BXGD014375 |
PROPERDIN DEFICIENCY, X-LINKED |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases |
| C1839630 |
BXGD014391 |
Severe muscular hypotonia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C1843505 |
BXGD014590 |
Degeneration of anterior horn cells |
Nervous System Diseases |
| C1851584 |
BXGD015221 |
Childhood Ependymoma |
Neoplasms |
| C1854657 |
BXGD015418 |
Limb fasciculations |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C1856694 |
BXGD015632 |
Areflexia of lower limbs |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C1858120 |
BXGD015774 |
Generalized hypotonia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C1858517 |
BXGD015802 |
SPINAL MUSCULAR ATROPHY WITH RESPIRATORY DISTRESS 1 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Nervous System Diseases |
| C1862941 |
BXGD016145 |
Amyotrophic Lateral Sclerosis, Sporadic |
Nutritional and Metabolic Diseases; Nervous System Diseases |
| C1864497 |
BXGD016232 |
PSORIASIS 2 |
|
| C1865384 |
BXGD016324 |
Amyotrophy, monomelic |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C1867441 |
BXGD016455 |
Pterygium Of Conjunctiva And Cornea |
Eye Diseases |
| C1959635 |
BXGD016646 |
Parvovirus B19 (disease) |
|
| C2004489 |
BXGD016873 |
Regurgitation |
|
| C2239176 |
BXGD016965 |
Liver carcinoma |
Digestive System Diseases; Neoplasms |
| C2242710 |
BXGD016997 |
Intra-Abdominal Hypertension |
Musculoskeletal Diseases; Cardiovascular Diseases |
| C2350019 |
BXGD017066 |
Solitary Pulmonary Nodule |
Respiratory Tract Diseases |
| C2711227 |
BXGD017478 |
Steatohepatitis |
Digestive System Diseases |
| C2747816 |
BXGD017577 |
Complicated malaria |
Infections |
| C2931358 |
BXGD018008 |
Muscular atrophy, spinal, infantile chronic form |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C2936380 |
BXGD018112 |
Neointima |
Pathological Conditions, Signs and Symptoms |
| C2937220 |
BXGD018154 |
Congenital abnormality of vein |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C3160718 |
BXGD018468 |
PARKINSON DISEASE, LATE-ONSET |
|
| C3203102 |
BXGD018555 |
Idiopathic pulmonary arterial hypertension |
Respiratory Tract Diseases |
| C3266262 |
BXGD018600 |
Multiple Chronic Conditions |
Pathological Conditions, Signs and Symptoms |
| C3489532 |
BXGD018934 |
Cone-Rod Dystrophy 2 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C3539878 |
BXGD019087 |
Triple Negative Breast Neoplasms |
Neoplasms; Skin and Connective Tissue Diseases |
| C3544347 |
BXGD019116 |
Intestinal fibrosis |
|
| C3642347 |
BXGD019246 |
Basal-Like Breast Carcinoma |
|
| C3661519 |
BXGD019264 |
Hereditary Motor Neuronopathy |
Nervous System Diseases |
| C3665732 |
BXGD019301 |
Metastatic Dermatofibrosarcoma Protuberans |
Neoplasms |
| C3826237 |
BXGD019718 |
Head--Tumors |
|
| C3840252 |
BXGD019796 |
Pseudomyogenic (epithelioid sarcoma-like) hemangioendothelioma |
|
| C3887461 |
BXGD019876 |
Head and Neck Carcinoma |
Neoplasms |
| C4016747 |
BXGD020369 |
SPINAL MUSCULAR ATROPHY, MODIFIER OF |
|
| C4024896 |
BXGD021461 |
Motor neuron atrophy |
|
| C4024911 |
BXGD021468 |
Acute infantile spinal muscular atrophy |
Nervous System Diseases |
| C4024957 |
BXGD021500 |
Proximal spinal muscular atrophy |
Nervous System Diseases |
| C4048328 |
BXGD021903 |
cervical cancer |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications |
| C4049993 |
BXGD021957 |
Aristolochic Acid Nephropathy |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C4086165 |
BXGD022126 |
Childhood Neuroblastoma |
Neoplasms |
| C4520843 |
BXGD023043 |
Pterygium of eye |
Eye Diseases |
| C4721438 |
BXGD023741 |
Mitral valve dysplasia |
Cardiovascular Diseases |
| C4721610 |
BXGD023760 |
Carcinoma, Ovarian Epithelial |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C4722518 |
BXGD023806 |
Triple-Negative Breast Carcinoma |
Neoplasms; Skin and Connective Tissue Diseases |
| C4722524 |
BXGD023807 |
Blood Vessel Tumors |
Neoplasms |
| C4732730 |
BXGD023895 |
Blood spots |
|
| C4732793 |
BXGD023902 |
Polyminimyoclonus |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C4750288 |
BXGD024069 |
Spinal muscular atrophy with lower extremity predominance |
Nervous System Diseases |