| C0000737 |
BXGD000005 |
Abdominal Pain |
Pathological Conditions, Signs and Symptoms |
| C0001948 |
BXGD000091 |
Alcohol consumption |
Behavior and Behavior Mechanisms |
| C0002171 |
BXGD000106 |
Alopecia Areata |
Skin and Connective Tissue Diseases |
| C0002395 |
BXGD000111 |
Alzheimer's Disease |
Nervous System Diseases; Mental Disorders |
| C0002736 |
BXGD000127 |
Amyotrophic Lateral Sclerosis |
Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0003467 |
BXGD000194 |
Anxiety |
Behavior and Behavior Mechanisms |
| C0003862 |
BXGD000230 |
Arthralgia |
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases |
| C0003868 |
BXGD000233 |
Arthritis, Gouty |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C0004096 |
BXGD000252 |
Asthma |
Respiratory Tract Diseases; Immune System Diseases |
| C0004134 |
BXGD000256 |
Ataxia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0004138 |
BXGD000258 |
Ataxias, Hereditary |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0004364 |
BXGD000270 |
Autoimmune Diseases |
Immune System Diseases |
| C0005612 |
BXGD000317 |
Birth Weight |
Pathological Conditions, Signs and Symptoms |
| C0005779 |
BXGD000336 |
Blood Coagulation Disorders |
Hemic and Lymphatic Diseases |
| C0005823 |
BXGD000339 |
Blood Pressure |
|
| C0005845 |
BXGD000341 |
Blood urea nitrogen measurement |
|
| C0005890 |
BXGD000345 |
Body Height |
|
| C0007102 |
BXGD000425 |
Malignant tumor of colon |
Digestive System Diseases; Neoplasms |
| C0007222 |
BXGD000454 |
Cardiovascular Diseases |
Cardiovascular Diseases |
| C0007570 |
BXGD000467 |
Celiac Disease |
Digestive System Diseases; Nutritional and Metabolic Diseases |
| C0007758 |
BXGD000475 |
Cerebellar Ataxia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0007760 |
BXGD000476 |
Cerebellar Diseases |
Nervous System Diseases |
| C0008312 |
BXGD000527 |
Primary biliary cirrhosis |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C0008313 |
BXGD000528 |
Cholangitis, Sclerosing |
Digestive System Diseases |
| C0008489 |
BXGD000546 |
Chorea |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0009324 |
BXGD000597 |
Ulcerative Colitis |
Digestive System Diseases |
| C0009375 |
BXGD000602 |
Colonic Neoplasms |
Digestive System Diseases; Neoplasms |
| C0009402 |
BXGD000605 |
Colorectal Carcinoma |
Digestive System Diseases; Neoplasms |
| C0009404 |
BXGD000606 |
Colorectal Neoplasms |
Digestive System Diseases; Neoplasms |
| C0009806 |
BXGD000633 |
Constipation |
Pathological Conditions, Signs and Symptoms |
| C0010068 |
BXGD000648 |
Coronary heart disease |
Cardiovascular Diseases |
| C0010346 |
BXGD000664 |
Crohn Disease |
Digestive System Diseases |
| C0011168 |
BXGD000700 |
Deglutition Disorders |
Digestive System Diseases; Otorhinolaryngologic Diseases |
| C0011265 |
BXGD000708 |
Presenile dementia |
Nervous System Diseases; Mental Disorders |
| C0011570 |
BXGD000729 |
Mental Depression |
Behavior and Behavior Mechanisms |
| C0011581 |
BXGD000733 |
Depressive disorder |
Mental Disorders |
| C0011854 |
BXGD000753 |
Diabetes Mellitus, Insulin-Dependent |
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases |
| C0011860 |
BXGD000755 |
Diabetes Mellitus, Non-Insulin-Dependent |
Nutritional and Metabolic Diseases; Endocrine System Diseases |
| C0012236 |
BXGD000772 |
DiGeorge Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases |
| C0013170 |
BXGD000802 |
Drug habituation |
Chemically-Induced Disorders; Mental Disorders |
| C0013362 |
BXGD000817 |
Dysarthria |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0013384 |
BXGD000826 |
Dyskinetic syndrome |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0013404 |
BXGD000833 |
Dyspnea |
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases |
| C0013421 |
BXGD000837 |
Dystonia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0013595 |
BXGD000858 |
Eczema |
Skin and Connective Tissue Diseases |
| C0014170 |
BXGD000902 |
Endometrial Neoplasms |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications |
| C0014772 |
BXGD000948 |
Red Blood Cell Count measurement |
|
| C0015644 |
BXGD001008 |
Muscular fasciculation |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0015672 |
BXGD001011 |
Fatigue |
Pathological Conditions, Signs and Symptoms |
| C0016719 |
BXGD001074 |
Friedreich Ataxia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0017168 |
BXGD001101 |
Gastroesophageal reflux disease |
Digestive System Diseases |
| C0017612 |
BXGD001129 |
Glaucoma, Open-Angle |
Eye Diseases |
| C0017654 |
BXGD001136 |
Glomerular Filtration Rate |
|
| C0018099 |
BXGD001172 |
Gout |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C0018213 |
BXGD001187 |
Graves Disease |
Eye Diseases; Immune System Diseases; Endocrine System Diseases |
| C0018790 |
BXGD001221 |
Cardiac Arrest |
Cardiovascular Diseases |
| C0018935 |
BXGD001252 |
Hematocrit procedure |
|
| C0019163 |
BXGD001295 |
Hepatitis B |
Digestive System Diseases; Infections |
| C0020179 |
BXGD001363 |
Huntington Disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders |
| C0020538 |
BXGD001422 |
Hypertensive disease |
Cardiovascular Diseases |
| C0020676 |
BXGD001462 |
Hypothyroidism |
Endocrine System Diseases |
| C0021053 |
BXGD001476 |
Immune System Diseases |
Immune System Diseases |
| C0021167 |
BXGD001487 |
Incontinence |
Nervous System Diseases |
| C0021390 |
BXGD001503 |
Inflammatory Bowel Diseases |
Digestive System Diseases |
| C0022336 |
BXGD001535 |
Creutzfeldt-Jakob disease |
Infections; Nervous System Diseases; Mental Disorders |
| C0022595 |
BXGD001562 |
Keratosis Follicularis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases |
| C0022661 |
BXGD001572 |
Kidney Failure, Chronic |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0023066 |
BXGD001605 |
Laryngospasm |
Respiratory Tract Diseases; Otorhinolaryngologic Diseases |
| C0023508 |
BXGD001675 |
White Blood Cell Count procedure |
|
| C0024141 |
BXGD001740 |
Lupus Erythematosus, Systemic |
Skin and Connective Tissue Diseases; Immune System Diseases |
| C0024408 |
BXGD001768 |
Machado-Joseph Disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0024528 |
BXGD001782 |
Malaise and fatigue |
|
| C0025517 |
BXGD001875 |
Metabolic Diseases |
Nutritional and Metabolic Diseases |
| C0026769 |
BXGD001930 |
Multiple Sclerosis |
Immune System Diseases; Nervous System Diseases |
| C0026827 |
BXGD001936 |
Muscle hypotonia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0026837 |
BXGD001937 |
Muscle Rigidity |
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases |
| C0026838 |
BXGD001938 |
Muscle Spasticity |
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases |
| C0026847 |
BXGD001940 |
Spinal Muscular Atrophy |
Nervous System Diseases |
| C0027022 |
BXGD001962 |
Myeloproliferative disease |
Hemic and Lymphatic Diseases |
| C0027051 |
BXGD001963 |
Myocardial Infarction |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0027066 |
BXGD001966 |
Myoclonus |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0027498 |
BXGD001994 |
Nausea and vomiting |
Pathological Conditions, Signs and Symptoms |
| C0027651 |
BXGD002009 |
Neoplasms |
Neoplasms |
| C0027746 |
BXGD002032 |
Nerve Degeneration |
Pathological Conditions, Signs and Symptoms |
| C0027765 |
BXGD002033 |
nervous system disorder |
Nervous System Diseases |
| C0027819 |
BXGD002043 |
Neuroblastoma |
Neoplasms |
| C0028738 |
BXGD002081 |
Nystagmus |
Eye Diseases; Nervous System Diseases |
| C0028754 |
BXGD002082 |
Obesity |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases |
| C0028968 |
BXGD002103 |
Olivopontocerebellar Atrophies |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0029089 |
BXGD002107 |
Ophthalmoplegia |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C0029124 |
BXGD002113 |
Optic Atrophy |
Eye Diseases; Nervous System Diseases |
| C0030193 |
BXGD002191 |
Pain |
Pathological Conditions, Signs and Symptoms |
| C0030567 |
BXGD002240 |
Parkinson Disease |
Nervous System Diseases |
| C0031117 |
BXGD002285 |
Peripheral Neuropathy |
Nervous System Diseases |
| C0032181 |
BXGD002332 |
Platelet Count measurement |
|
| C0032580 |
BXGD002362 |
Adenomatous Polyposis Coli |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms |
| C0033774 |
BXGD002419 |
Pruritus |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases |
| C0033860 |
BXGD002438 |
Psoriasis |
Skin and Connective Tissue Diseases |
| C0034152 |
BXGD002467 |
Henoch-Schoenlein Purpura |
Pathological Conditions, Signs and Symptoms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases |
| C0035258 |
BXGD002523 |
Restless Legs Syndrome |
Nervous System Diseases; Mental Disorders |
| C0035334 |
BXGD002539 |
Retinitis Pigmentosa |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C0036202 |
BXGD002581 |
Sarcoidosis |
Hemic and Lymphatic Diseases |
| C0036341 |
BXGD002600 |
Schizophrenia |
Mental Disorders |
| C0036572 |
BXGD002625 |
Seizures |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0037317 |
BXGD002689 |
Sleep disturbances |
Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0037369 |
BXGD002691 |
Smoking |
Behavior and Behavior Mechanisms |
| C0037763 |
BXGD002699 |
Spasm |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0037769 |
BXGD002701 |
West Syndrome |
Nervous System Diseases |
| C0037773 |
BXGD002704 |
Spastic Paraplegia, Hereditary |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0038002 |
BXGD002723 |
Splenomegaly |
Pathological Conditions, Signs and Symptoms |
| C0038013 |
BXGD002725 |
Ankylosing spondylitis |
Musculoskeletal Diseases |
| C0038436 |
BXGD002755 |
Post-Traumatic Stress Disorder |
Mental Disorders |
| C0038454 |
BXGD002760 |
Cerebrovascular accident |
Nervous System Diseases; Cardiovascular Diseases |
| C0038868 |
BXGD002781 |
Progressive supranuclear palsy |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C0039685 |
BXGD002825 |
Tetralogy of Fallot |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C0040822 |
BXGD002885 |
Tremor |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0042769 |
BXGD002999 |
Virus Diseases |
Infections |
| C0042798 |
BXGD003003 |
Low Vision |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C0042900 |
BXGD003012 |
Vitiligo |
Skin and Connective Tissue Diseases |
| C0043194 |
BXGD003036 |
Wiskott-Aldrich Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0043352 |
BXGD003045 |
Xerostomia |
Stomatognathic Diseases |
| C0085084 |
BXGD003121 |
Motor Neuron Disease |
Nervous System Diseases |
| C0085096 |
BXGD003123 |
Peripheral Vascular Diseases |
Cardiovascular Diseases |
| C0085278 |
BXGD003150 |
Antiphospholipid Syndrome |
Immune System Diseases |
| C0085606 |
BXGD003201 |
Urgency of micturition |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0085631 |
BXGD003214 |
Agitation |
Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0085633 |
BXGD003216 |
Mood swings |
Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0087012 |
BXGD003318 |
Ataxia, Spinocerebellar |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0087031 |
BXGD003319 |
Juvenile-Onset Still Disease |
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases |
| C0149782 |
BXGD003365 |
Squamous cell carcinoma of lung |
Neoplasms; Respiratory Tract Diseases |
| C0151888 |
BXGD003497 |
Hyporeflexia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0152013 |
BXGD003516 |
Adenocarcinoma of lung (disorder) |
Neoplasms |
| C0200633 |
BXGD004040 |
Neutrophil count (procedure) |
|
| C0200635 |
BXGD004041 |
Lymphocyte Count measurement |
|
| C0200637 |
BXGD004042 |
Monocyte count procedure |
|
| C0200638 |
BXGD004043 |
Eosinophil count procedure |
|
| C0200641 |
BXGD004044 |
Blood basophil count (lab test) |
|
| C0200665 |
BXGD004045 |
Platelet mean volume determination (procedure) |
|
| C0201910 |
BXGD004057 |
Beta-2-microglobulin measurement |
|
| C0202117 |
BXGD004074 |
Low density lipoprotein cholesterol measurement |
|
| C0202239 |
BXGD004087 |
Uric acid measurement (procedure) |
|
| C0205682 |
BXGD004105 |
Waist-Hip Ratio |
|
| C0206161 |
BXGD004167 |
Reticulocyte count (procedure) |
|
| C0206245 |
BXGD004173 |
Amyloid Neuropathies, Familial |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0221271 |
BXGD004431 |
Elastosis perforans serpiginosa |
Skin and Connective Tissue Diseases |
| C0231311 |
BXGD004491 |
Jet Lag Syndrome |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders |
| C0233565 |
BXGD004590 |
Bradykinesia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0234132 |
BXGD004623 |
Pyramidal sign |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0234133 |
BXGD004624 |
Extrapyramidal sign |
|
| C0234162 |
BXGD004627 |
Cerebellar Dysmetria |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0234366 |
BXGD004652 |
Ataxic |
|
| C0234376 |
BXGD004659 |
Action Tremor |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0234378 |
BXGD004661 |
Static Tremor |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0234379 |
BXGD004662 |
Resting Tremor |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0234979 |
BXGD004707 |
Dysdiadochokinesis |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0235025 |
BXGD004713 |
Peripheral motor neuropathy |
Nervous System Diseases |
| C0236642 |
BXGD004815 |
Pick Disease of the Brain |
Nervous System Diseases; Mental Disorders |
| C0240341 |
BXGD005032 |
Micrographia |
|
| C0240735 |
BXGD005052 |
Personality Change |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0241700 |
BXGD005108 |
Voice Fatigue |
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases |
| C0241910 |
BXGD005123 |
Autoimmune Chronic Hepatitis |
Digestive System Diseases; Immune System Diseases |
| C0242339 |
BXGD005150 |
Dyslipidemias |
Nutritional and Metabolic Diseases |
| C0242422 |
BXGD005163 |
Parkinsonian Disorders |
Nervous System Diseases |
| C0262404 |
BXGD005236 |
Cerebellar degeneration |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0264097 |
BXGD005365 |
Calcaneal apophysitis |
Skin and Connective Tissue Diseases; Musculoskeletal Diseases |
| C0264408 |
BXGD005387 |
Childhood asthma |
Respiratory Tract Diseases; Immune System Diseases |
| C0266617 |
BXGD005700 |
Congenital anomaly of face |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases |
| C0270736 |
BXGD006096 |
Essential Tremor |
Nervous System Diseases |
| C0271148 |
BXGD006165 |
Secondary Open Angle Glaucoma |
Eye Diseases |
| C0271270 |
BXGD006178 |
Oculovestibuloauditory syndrome |
Eye Diseases; Nervous System Diseases; Cardiovascular Diseases |
| C0271390 |
BXGD006198 |
Nystagmus, End-Position |
|
| C0337428 |
BXGD007155 |
Fibrinogen assay |
|
| C0338451 |
BXGD007176 |
Frontotemporal dementia |
Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders |
| C0338656 |
BXGD007211 |
Impaired cognition |
Mental Disorders |
| C0339573 |
BXGD007271 |
Glaucoma, Primary Open Angle |
Eye Diseases |
| C0344315 |
BXGD007666 |
Depressed mood |
Behavior and Behavior Mechanisms |
| C0346163 |
BXGD007785 |
Endometrioid carcinoma ovary |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C0346629 |
BXGD007831 |
Malignant neoplasm of large intestine |
Digestive System Diseases; Neoplasms |
| C0392885 |
BXGD008071 |
High density lipoprotein measurement |
|
| C0393525 |
BXGD008081 |
Progressive cerebellar ataxia |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0393554 |
BXGD008087 |
Amyotrophic Lateral Sclerosis With Dementia |
Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0393571 |
BXGD008094 |
Multiple System Atrophy |
Nervous System Diseases |
| C0393593 |
BXGD008103 |
Dystonia Disorders |
Nervous System Diseases |
| C0410702 |
BXGD008447 |
Adolescent idiopathic scoliosis |
Musculoskeletal Diseases |
| C0424448 |
BXGD008529 |
Mask-like facies |
Nervous System Diseases |
| C0424605 |
BXGD008535 |
Developmental delay (disorder) |
Mental Disorders |
| C0428474 |
BXGD008631 |
Serum LDL cholesterol measurement |
|
| C0428883 |
BXGD008639 |
Diastolic blood pressure |
|
| C0428886 |
BXGD008640 |
Mean blood pressure |
|
| C0442874 |
BXGD008814 |
Neuropathy |
Nervous System Diseases |
| C0449439 |
BXGD008820 |
Carrier status |
|
| C0476089 |
BXGD008977 |
Endometrial Carcinoma |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications |
| C0494479 |
BXGD009031 |
Other headache syndrome |
|
| C0497327 |
BXGD009061 |
Dementia |
Nervous System Diseases; Mental Disorders |
| C0518015 |
BXGD009068 |
Hemoglobin measurement |
|
| C0522224 |
BXGD009198 |
Paralysed |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0524587 |
BXGD009232 |
Mean Corpuscular Volume (result) |
|
| C0524851 |
BXGD009246 |
Neurodegenerative Disorders |
Nervous System Diseases |
| C0541794 |
BXGD009262 |
Skeletal muscle atrophy |
|
| C0543859 |
BXGD009298 |
Amyotrophic Lateral Sclerosis, Guam Form |
Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0546817 |
BXGD009342 |
Fluid overload |
Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Cardiovascular Diseases |
| C0557874 |
BXGD009444 |
Global developmental delay |
|
| C0566602 |
BXGD009489 |
Primary sclerosing cholangitis |
Digestive System Diseases |
| C0575090 |
BXGD009513 |
Equilibration disorder |
Nervous System Diseases |
| C0600139 |
BXGD009695 |
Prostate carcinoma |
Neoplasms; Male Urogenital Diseases |
| C0677607 |
BXGD009721 |
Hashimoto Disease |
Endocrine System Diseases |
| C0678222 |
BXGD009749 |
Breast Carcinoma |
Neoplasms; Skin and Connective Tissue Diseases |
| C0684249 |
BXGD009790 |
Carcinoma of lung |
Neoplasms; Respiratory Tract Diseases |
| C0700095 |
BXGD009875 |
Central neuroblastoma |
Neoplasms; Nervous System Diseases |
| C0700201 |
BXGD009880 |
Dyssomnias |
Nervous System Diseases; Mental Disorders |
| C0740279 |
BXGD009973 |
Cerebellar atrophy |
|
| C0746674 |
BXGD010147 |
Generalized muscle weakness |
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases |
| C0750880 |
BXGD010239 |
Monocyte count result |
|
| C0750937 |
BXGD010259 |
Ataxia, Appendicular |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0751072 |
BXGD010312 |
Frontotemporal Lobar Degeneration |
Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders |
| C0751401 |
BXGD010427 |
Ophthalmoparesis |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C0751706 |
BXGD010559 |
Primary Progressive Nonfluent Aphasia |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders |
| C0751778 |
BXGD010587 |
Myoclonic Epilepsies, Progressive |
Nervous System Diseases |
| C0751781 |
BXGD010590 |
Dentatorubral-Pallidoluysian Atrophy |
Nervous System Diseases |
| C0751785 |
BXGD010594 |
Unverricht-Lundborg Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0751837 |
BXGD010604 |
Gait Ataxia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0752098 |
BXGD010660 |
Autosomal Dominant Parkinsonism |
Nervous System Diseases |
| C0752120 |
BXGD010668 |
Spinocerebellar Ataxia Type 1 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0752121 |
BXGD010669 |
Spinocerebellar Ataxia Type 2 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0752122 |
BXGD010670 |
Spinocerebellar Ataxia Type 4 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0752123 |
BXGD010671 |
Spinocerebellar Ataxia Type 5 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0752124 |
BXGD010672 |
Spinocerebellar Ataxia Type 6 (disorder) |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0752125 |
BXGD010673 |
Spinocerebellar Ataxia Type 7 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0851578 |
BXGD010925 |
Sleep Disorders |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders |
| C0857490 |
BXGD011150 |
Granulocyte count |
|
| C0871470 |
BXGD011316 |
Systolic Pressure |
|
| C0917798 |
BXGD011409 |
Cerebral Ischemia |
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 |
| C1112256 |
BXGD011655 |
Sensorimotor neuropathy |
|
| C1142166 |
BXGD011736 |
Brugada Syndrome (disorder) |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C1145670 |
BXGD011764 |
Respiratory Failure |
Respiratory Tract Diseases |
| C1261473 |
BXGD011855 |
Sarcoma |
Neoplasms |
| C1261502 |
BXGD011856 |
Finding of Mean Corpuscular Hemoglobin |
|
| C1272321 |
BXGD012011 |
Autoantibody measurement |
|
| C1295585 |
BXGD012241 |
Decreased vibratory sense |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C1302401 |
BXGD012303 |
Adenoma of large intestine |
Digestive System Diseases; Neoplasms |
| C1305849 |
BXGD012347 |
Diastolic blood pressure measurement |
|
| C1305855 |
BXGD012348 |
Body mass index |
|
| C1306620 |
BXGD012371 |
Systolic blood pressure measurement |
|
| C1319315 |
BXGD012415 |
Adenocarcinoma of large intestine |
Digestive System Diseases; Neoplasms |
| C1321329 |
BXGD012430 |
Slowed saccades |
|
| C1332355 |
BXGD012529 |
Autoimmune Hepatitis with Centrilobular Necrosis |
|
| C1335177 |
BXGD012771 |
Ovarian Serous Adenocarcinoma |
Neoplasms |
| C1367972 |
BXGD012891 |
Phlebitis and thrombophlebitis |
Cardiovascular Diseases |
| C1384600 |
BXGD012945 |
Systemic onset juvenile chronic arthritis |
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases |
| C1384666 |
BXGD012948 |
hearing impairment |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases |
| C1395088 |
BXGD012988 |
Nervous system--Degeneration |
|
| C1408507 |
BXGD013038 |
Supranuclear ophthalmoplegia |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C1445957 |
BXGD013081 |
Serum total cholesterol measurement |
|
| C1527304 |
BXGD013266 |
Allergic Reaction |
Immune System Diseases |
| C1561643 |
BXGD013363 |
Chronic Kidney Diseases |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C1611743 |
BXGD013456 |
Familial (FPAH) |
|
| C1619716 |
BXGD013461 |
Cystatin C measurement |
|
| C1704436 |
BXGD013564 |
Peripheral Arterial Diseases |
Cardiovascular Diseases |
| C1739108 |
BXGD013730 |
Latent Autoimmune Diabetes in Adults |
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases |
| C1836392 |
BXGD014111 |
Dysmetric saccades |
|
| C1836824 |
BXGD014163 |
Amish Infantile Epilepsy Syndrome |
Nervous System Diseases |
| C1837315 |
BXGD014218 |
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 |
|
| C1837461 |
BXGD014234 |
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 |
|
| C1839259 |
BXGD014363 |
Bulbo-Spinal Atrophy, X-Linked |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C1843663 |
BXGD014600 |
Urinary bladder sphincter dysfunction |
|
| C1843792 |
BXGD014606 |
FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED |
|
| C1843921 |
BXGD014620 |
Postural instability |
Nervous System Diseases |
| C1846176 |
BXGD014791 |
Hyperactive deep tendon reflexes |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C1846865 |
BXGD014845 |
Substantia nigra gliosis |
Pathological Conditions, Signs and Symptoms |
| C1847117 |
BXGD014852 |
Dilated fourth ventricle |
|
| C1847987 |
BXGD014900 |
HUNTINGTON DISEASE-LIKE 2 |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders |
| C1848736 |
BXGD014970 |
Distal amyotrophy |
|
| C1850496 |
BXGD015147 |
Neuronal loss in central nervous system |
|
| C1853237 |
BXGD015319 |
Isolated cases |
|
| C1856019 |
BXGD015564 |
Abnormal cortical gyration |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C1858120 |
BXGD015774 |
Generalized hypotonia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C1858558 |
BXGD015806 |
Rheumatoid Arthritis, Systemic Juvenile |
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases |
| C1859341 |
BXGD015878 |
Olivopontocerebellar hypoplasia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders |
| C1862941 |
BXGD016145 |
Amyotrophic Lateral Sclerosis, Sporadic |
Nutritional and Metabolic Diseases; Nervous System Diseases |
| C1866751 |
BXGD016422 |
Spinocerebellar tract degeneration |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C1866753 |
BXGD016423 |
Impaired horizontal smooth pursuit |
|
| C1868684 |
BXGD016527 |
EAR, PATELLA, SHORT STATURE SYNDROME |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases |
| C1956346 |
BXGD016627 |
Coronary Artery Disease |
Cardiovascular Diseases |
| C1963060 |
BXGD016679 |
Agitation, CTCAE 3.0 |
|
| C1963184 |
BXGD016688 |
Nystagmus, CTCAE 3.0 |
|
| C1963674 |
BXGD016692 |
Spinocerebellar Ataxia 10 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C1997740 |
BXGD016863 |
Segmental dystonia |
Nervous System Diseases |
| C2242712 |
BXGD016999 |
Hyper LDL cholesterolaemia |
|
| C2607914 |
BXGD017148 |
Allergic rhinitis (disorder) |
Respiratory Tract Diseases; Immune System Diseases; Otorhinolaryngologic Diseases |
| C2675481 |
BXGD017292 |
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 |
|
| C2677123 |
BXGD017364 |
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 |
|
| C2718017 |
BXGD017522 |
TDP-43 Proteinopathies |
Nutritional and Metabolic Diseases; Nervous System Diseases |
| C2751492 |
BXGD017718 |
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C2931171 |
BXGD017967 |
Juvenile pauciarticular chronic arthritis |
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases |
| C2985280 |
BXGD018223 |
Blood Protein Measurement |
|
| C3149907 |
BXGD018288 |
AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 13 |
|
| C3160718 |
BXGD018468 |
PARKINSON DISEASE, LATE-ONSET |
|
| C3266262 |
BXGD018600 |
Multiple Chronic Conditions |
Pathological Conditions, Signs and Symptoms |
| C3277671 |
BXGD018715 |
THROMBOCYTHEMIA 1 |
|
| C3489733 |
BXGD018945 |
Oculomotor apraxia |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases; Behavior and Behavior Mechanisms; Cardiovascular Diseases |
| C3489791 |
BXGD018949 |
Parkinson Disease, Familial, Type 1 |
Nervous System Diseases |
| C3495559 |
BXGD018994 |
Juvenile arthritis |
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases |
| C3554460 |
BXGD019215 |
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 |
|
| C3711380 |
BXGD019386 |
Huntington Disease-Like Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C3805043 |
BXGD019457 |
Vascular cognitive impairment |
|
| C3805715 |
BXGD019484 |
Short stepped shuffling gait |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C3811918 |
BXGD019664 |
GRN-related frontotemporal dementia |
Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders |
| C3828530 |
BXGD019744 |
Platelet Component Distribution Width Measurement |
|
| C3887485 |
BXGD019877 |
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1 |
|
| C3887898 |
BXGD019926 |
Infantile Spasm |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C3890205 |
BXGD020020 |
Polyarticular Juvenile Idiopathic Arthritis, Rheumatoid Factor Negative |
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases |
| C3898105 |
BXGD020059 |
Oligoarticular Juvenile Idiopathic Arthritis |
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases |
| C4022403 |
BXGD020897 |
Abnormality of the substantia nigra |
|
| C4022587 |
BXGD020928 |
Fatigable weakness of respiratory muscles |
|
| C4022588 |
BXGD020929 |
Fatigable weakness of swallowing muscles |
|
| C4022735 |
BXGD020971 |
Cerebral white matter atrophy |
Pathological Conditions, Signs and Symptoms |
| C4023053 |
BXGD021086 |
Cerebellar Purkinje layer atrophy |
|
| C4024706 |
BXGD021379 |
Spinal cord posterior columns myelin loss |
|
| C4024900 |
BXGD021463 |
Atrophy/Degeneration affecting the brainstem |
|
| C4025647 |
BXGD021708 |
Abnormality of the spinocerebellar tracts |
|
| C4086165 |
BXGD022126 |
Childhood Neuroblastoma |
Neoplasms |
| C4087347 |
BXGD022144 |
Autosomal dominant cerebellar ataxia |
|
| C4302185 |
BXGD022525 |
Atypical Parkinsonism |
Nervous System Diseases |
| C4476793 |
BXGD022872 |
Abnormal cell morphology |
|
| C4518339 |
BXGD023019 |
Sporadic adult-onset ataxia of unknown etiology |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C4528257 |
BXGD023159 |
Corpuscular Hemoglobin Concentration Mean |
|
| C4551520 |
BXGD023336 |
Intention tremor |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C4551521 |
BXGD023337 |
Kinetic tremor |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C4551583 |
BXGD023361 |
Cerebral cortical atrophy |
|
| C4551637 |
BXGD023379 |
Erythrocytosis familial, 1 |
Hemic and Lymphatic Diseases |
| C4551686 |
BXGD023391 |
Malignant neoplasm of soft tissue |
Neoplasms |
| C4551714 |
BXGD023398 |
Rod-Cone Dystrophy |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C4551993 |
BXGD023469 |
Amyotrophic Lateral Sclerosis, Familial |
Nutritional and Metabolic Diseases; Nervous System Diseases |
| C4552811 |
BXGD023526 |
Generalized Muscle Weakness, CTCAE |
|
| C4552855 |
BXGD023528 |
Agitation, CTCAE 5.0 |
|
| C4553743 |
BXGD023548 |
Spasticity, CTCAE |
|
| C4553976 |
BXGD023554 |
Urinary Urgency, CTCAE 5 |
|
| C4554036 |
BXGD023557 |
Nystagmus, CTCAE 5.0 |
|
| C4721453 |
BXGD023744 |
Peripheral Nervous System Diseases |
Nervous System Diseases |