Showing entry for Prelamin-A/C


　 　 　 　 　 　 　 　 　 　 　 　
General Target Information
BXGT IdBXGT005889
Protein NamePrelamin-A/C
Uniport IdP02545
GeneLMNA
Gene Id4000
DomainFilament; LTD
Pfam PF00038   PF00932  
OrganismHomo sapiens (Human)
Target protein  affiliated  biological  pathways
KEGG
Class Subclass KEGG Id Pathway Name
4. Cellular Processes 4.2 Cell growth and death hsa04210 Apoptosis
6. Human Diseases 6.6 Cardiovascular diseases hsa05410 Hypertrophic cardiomyopathy (HCM)
6. Human Diseases 6.6 Cardiovascular diseases hsa05412 Arrhythmogenic right ventricular cardiomyopathy (ARVC)
6. Human Diseases 6.6 Cardiovascular diseases hsa05414 Dilated cardiomyopathy (DCM)
Gene Ontology
GO Type GO Id Gene Ontology
Biological Process GO:0034613 cellular protein localization
Biological Process GO:0071456 cellular response to hypoxia
Biological Process GO:0030951 establishment or maintenance of microtubule cytoskeleton polarity
Biological Process GO:0036498 IRE1-mediated unfolded protein response
Biological Process GO:0007084 mitotic nuclear envelope reassembly
Biological Process GO:0007517 muscle organ development
Biological Process GO:1903243 negative regulation of cardiac muscle hypertrophy in response to stress
Biological Process GO:0008285 negative regulation of cell population proliferation
Biological Process GO:2001237 negative regulation of extrinsic apoptotic signaling pathway
Biological Process GO:0072201 negative regulation of mesenchymal cell proliferation
Biological Process GO:0090201 negative regulation of release of cytochrome c from mitochondria
Biological Process GO:0006998 nuclear envelope organization
Biological Process GO:0090343 positive regulation of cell aging
Biological Process GO:0010628 positive regulation of gene expression
Biological Process GO:1900114 positive regulation of histone H3-K9 trimethylation
Biological Process GO:0006606 protein import into nucleus
Biological Process GO:0034504 protein localization to nucleus
Biological Process GO:0030334 regulation of cell migration
Biological Process GO:1900180 regulation of protein localization to nucleus
Biological Process GO:0031647 regulation of protein stability
Biological Process GO:0032204 regulation of telomere maintenance
Biological Process GO:0055015 ventricular cardiac muscle cell development
molecular function GO:0042802 identical protein binding
molecular function GO:0005198 structural molecule activity
cellular component GO:0005829 cytosol
cellular component GO:0005882 intermediate filament
cellular component GO:0005638 lamin filament
cellular component GO:0016604 nuclear body
cellular component GO:0005635 nuclear envelope
cellular component GO:0005652 nuclear lamina
cellular component GO:0031965 nuclear membrane
cellular component GO:0016607 nuclear speck
cellular component GO:0005654 nucleoplasm
cellular component GO:0005634 nucleus
cellular component GO:0048471 perinuclear region of cytoplasm
Reactome
Pathway Id Pathway Name
R-HSA-1643685 Disease
R-HSA-381038 XBP1(S) activates chaperone genes
R-HSA-381070 IRE1alpha activates chaperones
R-HSA-381119 Unfolded Protein Response (UPR)
R-HSA-392499 Metabolism of proteins
R-HSA-5663202 Diseases of signal transduction by growth factor receptors and second messengers
R-HSA-6802952 Signaling by BRAF and RAF fusions
R-HSA-6802957 Oncogenic MAPK signaling
Target protein-related  diseases
Disease
CUI Id BXGD Id Disease Name Disease Class
C0000768 BXGD000007 Congenital Abnormality Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C0000889 BXGD000018 Acanthosis Nigricans Skin and Connective Tissue Diseases
C0001339 BXGD000041 Acute pancreatitis Digestive System Diseases
C0001418 BXGD000050 Adenocarcinoma Neoplasms
C0001787 BXGD000076 Osteoporosis, Age-Related Nutritional and Metabolic Diseases; Musculoskeletal Diseases
C0002170 BXGD000105 Alopecia Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
C0002312 BXGD000107 alpha-Thalassemia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
C0002395 BXGD000111 Alzheimer's Disease Nervous System Diseases; Mental Disorders
C0002962 BXGD000160 Angina Pectoris Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0003090 BXGD000175 Ankylosis Musculoskeletal Diseases
C0003507 BXGD000203 Aortic Valve Stenosis Cardiovascular Diseases
C0003811 BXGD000222 Cardiac Arrhythmia Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0003850 BXGD000225 Arteriosclerosis Cardiovascular Diseases
C0003862 BXGD000230 Arthralgia Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases
C0003873 BXGD000236 Rheumatoid Arthritis Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases
C0003886 BXGD000238 Arthrogryposis Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0004153 BXGD000260 Atherosclerosis Cardiovascular Diseases
C0004238 BXGD000262 Atrial Fibrillation Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0004239 BXGD000263 Atrial Flutter Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0004245 BXGD000264 Atrioventricular Block Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0004331 BXGD000268 Auriculo-Ventricular Dissociation Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0004364 BXGD000270 Autoimmune Diseases Immune System Diseases
C0004604 BXGD000278 Back Pain Pathological Conditions, Signs and Symptoms
C0004779 BXGD000291 Basal Cell Nevus Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
C0005744 BXGD000330 Blepharophimosis Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
C0005745 BXGD000331 Blepharoptosis Eye Diseases
C0005890 BXGD000345 Body Height
C0005940 BXGD000352 Bone Diseases Musculoskeletal Diseases
C0006118 BXGD000372 Brain Neoplasms Neoplasms; Nervous System Diseases
C0006142 BXGD000374 Malignant neoplasm of breast Neoplasms; Skin and Connective Tissue Diseases
C0006625 BXGD000401 Cachexia Pathological Conditions, Signs and Symptoms
C0006663 BXGD000403 Calcinosis Nutritional and Metabolic Diseases
C0006826 BXGD000408 Malignant Neoplasms Neoplasms
C0007097 BXGD000424 Carcinoma Neoplasms
C0007102 BXGD000425 Malignant tumor of colon Digestive System Diseases; Neoplasms
C0007103 BXGD000426 Malignant neoplasm of endometrium Neoplasms; Female Urogenital Diseases and Pregnancy Complications
C0007112 BXGD000429 Adenocarcinoma of prostate Neoplasms; Male Urogenital Diseases
C0007114 BXGD000431 Malignant neoplasm of skin Neoplasms; Skin and Connective Tissue Diseases
C0007124 BXGD000437 Noninfiltrating Intraductal Carcinoma Neoplasms
C0007130 BXGD000440 Mucinous Adenocarcinoma Neoplasms
C0007133 BXGD000442 Carcinoma, Papillary Neoplasms
C0007134 BXGD000443 Renal Cell Carcinoma Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0007137 BXGD000445 Squamous cell carcinoma Neoplasms
C0007138 BXGD000446 Carcinoma, Transitional Cell Neoplasms
C0007193 BXGD000451 Cardiomyopathy, Dilated Cardiovascular Diseases
C0007194 BXGD000452 Hypertrophic Cardiomyopathy Cardiovascular Diseases
C0007196 BXGD000453 Restrictive cardiomyopathy Cardiovascular Diseases
C0007222 BXGD000454 Cardiovascular Diseases Cardiovascular Diseases
C0007282 BXGD000458 Carotid Stenosis Nervous System Diseases; Cardiovascular Diseases
C0007642 BXGD000469 Cellulitis Pathological Conditions, Signs and Symptoms; Infections; Skin and Connective Tissue Diseases
C0007787 BXGD000487 Transient Ischemic Attack Nervous System Diseases; Cardiovascular Diseases
C0007959 BXGD000507 Charcot-Marie-Tooth Disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0008297 BXGD000522 Choanal Atresia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Otorhinolaryngologic Diseases
C0008311 BXGD000526 Cholangitis Digestive System Diseases
C0008626 BXGD000559 Congenital chromosomal disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C0008928 BXGD000576 Cleidocranial Dysplasia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0009207 BXGD000593 Cockayne Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases
C0009319 BXGD000596 Colitis Digestive System Diseases
C0009402 BXGD000605 Colorectal Carcinoma Digestive System Diseases; Neoplasms
C0009681 BXGD000621 Anomalous pulmonary artery Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases
C0009917 BXGD000635 Contracture Musculoskeletal Diseases
C0009918 BXGD000636 Contracture of joint Musculoskeletal Diseases
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
C0010520 BXGD000675 Cyanosis Pathological Conditions, Signs and Symptoms
C0010606 BXGD000677 Adenoid Cystic Carcinoma Neoplasms
C0010674 BXGD000683 Cystic Fibrosis Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Respiratory Tract Diseases
C0010823 BXGD000690 Cytomegalovirus Infections Infections
C0011195 BXGD000702 Dejerine-Sottas Disease (disorder) Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0011265 BXGD000708 Presenile dementia Nervous System Diseases; Mental Disorders
C0011644 BXGD000744 Scleroderma Skin and Connective Tissue Diseases
C0011813 BXGD000748 Dextrocardia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C0011847 BXGD000749 Diabetes Endocrine System Diseases
C0011849 BXGD000751 Diabetes Mellitus Nutritional and Metabolic Diseases; Endocrine System Diseases
C0011860 BXGD000755 Diabetes Mellitus, Non-Insulin-Dependent Nutritional and Metabolic Diseases; Endocrine System Diseases
C0011881 BXGD000760 Diabetic Nephropathy Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases
C0012624 BXGD000780 Discitis Infections; Musculoskeletal Diseases
C0013274 BXGD000809 Patent ductus arteriosus Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C0013336 BXGD000815 Dwarfism Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases
C0013384 BXGD000826 Dyskinetic syndrome Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0013390 BXGD000828 Dysmenorrhea Pathological Conditions, Signs and Symptoms
C0013537 BXGD000853 Eclampsia Female Urogenital Diseases and Pregnancy Complications
C0013990 BXGD000874 Pathological accumulation of air in tissues Pathological Conditions, Signs and Symptoms
C0014390 BXGD000913 Entropion Eye Diseases
C0014518 BXGD000921 Toxic Epidermal Necrolysis Skin and Connective Tissue Diseases; Immune System Diseases; Chemically-Induced Disorders; Stomatognathic Diseases
C0014544 BXGD000926 Epilepsy Nervous System Diseases
C0014547 BXGD000927 Epilepsies, Partial Nervous System Diseases
C0014848 BXGD000955 Esophageal Achalasia Digestive System Diseases
C0015300 BXGD000973 Exophthalmos Eye Diseases
C0015544 BXGD001003 Failure to Thrive Pathological Conditions, Signs and Symptoms
C0015695 BXGD001013 Fatty Liver Digestive System Diseases
C0015934 BXGD001026 Fetal Growth Retardation Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications
C0015944 BXGD001028 Fetal Membranes, Premature Rupture Female Urogenital Diseases and Pregnancy Complications
C0016202 BXGD001050 Flatfoot Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0016506 BXGD001062 Foot Deformities Musculoskeletal Diseases
C0016508 BXGD001063 Congenital Foot Deformity Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0016667 BXGD001072 Fragile X Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0016842 BXGD001083 Congenital pectus excavatum Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0017636 BXGD001131 Glioblastoma Neoplasms
C0017668 BXGD001143 Focal glomerulosclerosis Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0017979 BXGD001159 Glycosuria Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0018566 BXGD001205 Congenital Hand Deformities Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0018784 BXGD001220 Sensorineural Hearing Loss (disorder) Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
C0018790 BXGD001221 Cardiac Arrest Cardiovascular Diseases
C0018794 BXGD001222 Heart Block Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0018798 BXGD001223 Congenital Heart Defects Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C0018799 BXGD001224 Heart Diseases Cardiovascular Diseases
C0018801 BXGD001226 Heart failure Cardiovascular Diseases
C0018802 BXGD001227 Congestive heart failure Cardiovascular Diseases
C0018817 BXGD001235 Atrial Septal Defects Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C0019100 BXGD001283 Severe Dengue Infections
C0019163 BXGD001295 Hepatitis B Digestive System Diseases; Infections
C0019209 BXGD001305 Hepatomegaly Pathological Conditions, Signs and Symptoms; Digestive System Diseases
C0019270 BXGD001311 Hernia Pathological Conditions, Signs and Symptoms
C0019348 BXGD001325 Herpes Simplex Infections Infections; Skin and Connective Tissue Diseases
C0019572 BXGD001338 Hirsutism Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
C0020179 BXGD001363 Huntington Disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders
C0020224 BXGD001366 Polyhydramnios Female Urogenital Diseases and Pregnancy Complications
C0020443 BXGD001385 Hypercholesterolemia Nutritional and Metabolic Diseases
C0020456 BXGD001392 Hyperglycemia Nutritional and Metabolic Diseases
C0020459 BXGD001394 Hyperinsulinism Nutritional and Metabolic Diseases
C0020473 BXGD001396 Hyperlipidemia Nutritional and Metabolic Diseases
C0020490 BXGD001403 Hyperopia Eye Diseases
C0020534 BXGD001421 Orbital separation excessive Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0020538 BXGD001422 Hypertensive disease Cardiovascular Diseases
C0020557 BXGD001432 Hypertriglyceridemia Nutritional and Metabolic Diseases
C0020608 BXGD001443 Hypodontia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases
C0020619 BXGD001447 Hypogonadism Endocrine System Diseases
C0020620 BXGD001448 Hypohidrosis Skin and Connective Tissue Diseases
C0020678 BXGD001463 Hypotrichosis Skin and Connective Tissue Diseases
C0020725 BXGD001465 Type II Mucolipidosis Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases
C0020757 BXGD001466 Ichthyoses Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C0021051 BXGD001475 Immunologic Deficiency Syndromes Immune System Diseases
C0021053 BXGD001476 Immune System Diseases Immune System Diseases
C0021122 BXGD001481 Disruptive, Impulse Control, and Conduct Disorders Mental Disorders
C0021359 BXGD001498 Infertility Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0021367 BXGD001501 Mammary Ductal Carcinoma Neoplasms; Skin and Connective Tissue Diseases
C0021390 BXGD001503 Inflammatory Bowel Diseases Digestive System Diseases
C0021655 BXGD001508 Insulin Resistance Nutritional and Metabolic Diseases
C0021775 BXGD001512 Intermittent Claudication Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0022408 BXGD001544 Arthropathy Musculoskeletal Diseases
C0022575 BXGD001555 Keratoconjunctivitis Sicca Eye Diseases
C0022602 BXGD001564 Actinic keratosis Neoplasms; Skin and Connective Tissue Diseases
C0022658 BXGD001570 Kidney Diseases Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0022661 BXGD001572 Kidney Failure, Chronic Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0022665 BXGD001573 Kidney Neoplasm Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0022821 BXGD001590 Kyphosis deformity of spine Musculoskeletal Diseases
C0023418 BXGD001642 leukemia Neoplasms
C0023449 BXGD001650 Acute lymphocytic leukemia Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0023452 BXGD001651 Childhood Acute Lymphoblastic Leukemia Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0023473 BXGD001661 Myeloid Leukemia, Chronic Neoplasms; Hemic and Lymphatic Diseases
C0023487 BXGD001669 Acute Promyelocytic Leukemia Neoplasms
C0023508 BXGD001675 White Blood Cell Count procedure
C0023787 BXGD001698 Lipodystrophy Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
C0023891 BXGD001714 Liver Cirrhosis, Alcoholic Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Chemically-Induced Disorders
C0023895 BXGD001717 Liver diseases Digestive System Diseases
C0023903 BXGD001720 Liver neoplasms Digestive System Diseases; Neoplasms
C0024003 BXGD001726 Lordosis Musculoskeletal Diseases
C0024121 BXGD001735 Lung Neoplasms Neoplasms; Respiratory Tract Diseases
C0024141 BXGD001740 Lupus Erythematosus, Systemic Skin and Connective Tissue Diseases; Immune System Diseases
C0024299 BXGD001758 Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0024305 BXGD001763 Lymphoma, Non-Hodgkin Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0025286 BXGD001850 Meningioma Neoplasms; Nervous System Diseases
C0025322 BXGD001863 Premature Menopause Female Urogenital Diseases and Pregnancy Complications
C0025517 BXGD001875 Metabolic Diseases Nutritional and Metabolic Diseases
C0025990 BXGD001884 Micrognathism Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases
C0026034 BXGD001887 Microstomia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases
C0026266 BXGD001895 Mitral Valve Insufficiency Cardiovascular Diseases
C0026267 BXGD001896 Mitral Valve Prolapse Syndrome Cardiovascular Diseases
C0026640 BXGD001912 Mouth Neoplasms Neoplasms; Stomatognathic Diseases
C0026769 BXGD001930 Multiple Sclerosis Immune System 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
C0026837 BXGD001937 Muscle Rigidity Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
C0026847 BXGD001940 Spinal Muscular Atrophy Nervous System Diseases
C0026848 BXGD001941 Myopathy Musculoskeletal Diseases; Nervous System Diseases
C0026850 BXGD001942 Muscular Dystrophy Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C0027051 BXGD001963 Myocardial Infarction Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0027121 BXGD001973 Myositis Musculoskeletal Diseases; Nervous System Diseases
C0027125 BXGD001975 Myotonia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0027443 BXGD001992 Natal Teeth
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
C0027888 BXGD002056 Hereditary Motor and Sensory Neuropathies Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0028754 BXGD002082 Obesity Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases
C0029408 BXGD002137 Degenerative polyarthritis Musculoskeletal Diseases
C0029453 BXGD002154 Osteopenia Nutritional and Metabolic Diseases; Musculoskeletal Diseases
C0029456 BXGD002157 Osteoporosis Nutritional and Metabolic Diseases; Musculoskeletal Diseases
C0029459 BXGD002159 Osteoporosis, Senile Nutritional and Metabolic Diseases; Musculoskeletal Diseases
C0029463 BXGD002160 Osteosarcoma Neoplasms
C0029882 BXGD002177 Otitis Media Otorhinolaryngologic Diseases
C0030305 BXGD002206 Pancreatitis Digestive System Diseases
C0030499 BXGD002232 Parasitic Diseases Infections
C0030552 BXGD002238 Paresis Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0030567 BXGD002240 Parkinson Disease Nervous System Diseases
C0030779 BXGD002252 Pelger-Huet Anomaly Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
C0031039 BXGD002274 Pericardial effusion Cardiovascular Diseases
C0031117 BXGD002285 Peripheral Neuropathy Nervous System Diseases
C0031212 BXGD002295 Personality Disorders Mental Disorders
C0032227 BXGD002336 Pleural effusion disorder Respiratory Tract Diseases
C0032460 BXGD002355 Polycystic Ovary Syndrome Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
C0032708 BXGD002368 Disorders of Porphyrin Metabolism Nutritional and Metabolic Diseases
C0033300 BXGD002403 Progeria Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
C0033377 BXGD002406 Ptosis Pathological Conditions, Signs and Symptoms
C0033626 BXGD002412 Protein Deficiency Nutritional and Metabolic Diseases
C0034012 BXGD002449 Delayed Puberty Endocrine System Diseases
C0034013 BXGD002450 Precocious Puberty Endocrine System Diseases
C0034069 BXGD002458 Pulmonary Fibrosis Respiratory Tract Diseases
C0035229 BXGD002516 Respiratory Insufficiency Respiratory Tract Diseases
C0035304 BXGD002528 Retinal Degeneration Eye Diseases
C0035335 BXGD002540 Retinoblastoma Neoplasms; Eye Diseases
C0036420 BXGD002612 Localized scleroderma Skin and Connective Tissue Diseases
C0036421 BXGD002613 Systemic Scleroderma Skin and Connective Tissue Diseases
C0036439 BXGD002615 Scoliosis, unspecified Musculoskeletal Diseases
C0036572 BXGD002625 Seizures Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0036646 BXGD002627 Age-related cataract Eye Diseases
C0037052 BXGD002662 Sick Sinus Syndrome Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0037188 BXGD002669 Sinoatrial Block Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0037268 BXGD002675 Skin Abnormalities Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C0037274 BXGD002676 Dermatologic disorders Skin and Connective Tissue Diseases
C0037286 BXGD002681 Skin Neoplasms Neoplasms; Skin and Connective Tissue Diseases
C0037299 BXGD002685 Skin Ulcer Skin and Connective Tissue Diseases
C0037301 BXGD002686 Skin Wrinkling
C0037317 BXGD002689 Sleep disturbances Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
C0037579 BXGD002694 Soft Tissue Neoplasms Neoplasms
C0038002 BXGD002723 Splenomegaly Pathological Conditions, Signs and Symptoms
C0038436 BXGD002755 Post-Traumatic Stress Disorder Mental Disorders
C0039070 BXGD002787 Syncope Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0039075 BXGD002788 Syndactyly Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0039239 BXGD002803 Sinus Tachycardia Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0039240 BXGD002804 Supraventricular tachycardia Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0039273 BXGD002806 Talipes cavus Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0039483 BXGD002813 Giant Cell Arteritis Skin and Connective Tissue Diseases; Immune System Diseases; Nervous System Diseases; Cardiovascular Diseases
C0040136 BXGD002845 Thyroid Neoplasm Neoplasms; Endocrine System Diseases
C0040433 BXGD002865 Tooth Crowding Stomatognathic Diseases
C0040761 BXGD002883 Transposition of Great Vessels Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C0042373 BXGD002978 Vascular Diseases Cardiovascular Diseases
C0042510 BXGD002987 Ventricular Fibrillation Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0042514 BXGD002989 Tachycardia, Ventricular Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0042900 BXGD003012 Vitiligo Skin and Connective Tissue Diseases
C0042928 BXGD003014 Vocal Cord Paralysis Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases
C0042963 BXGD003018 Vomiting Pathological Conditions, Signs and Symptoms
C0043119 BXGD003029 Werner Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
C0043325 BXGD003041 Xanthomatosis Nutritional and Metabolic Diseases
C0079035 BXGD003061 Bradyarrhythmia (disorder) Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0079744 BXGD003090 Diffuse Large B-Cell Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0085110 BXGD003126 Severe Combined Immunodeficiency Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases
C0085207 BXGD003140 Gestational Diabetes Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
C0085280 BXGD003151 Alagille Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Cardiovascular Diseases
C0085298 BXGD003155 Sudden Cardiac Death Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0085409 BXGD003168 Polyendocrinopathies, Autoimmune Immune System Diseases; Endocrine System Diseases
C0085612 BXGD003204 Ventricular arrhythmia Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0085681 BXGD003237 Hyperphosphatemia (disorder) Nutritional and Metabolic Diseases
C0085750 BXGD003249 Adenosis of Breast Skin and Connective Tissue Diseases
C0086543 BXGD003294 Cataract Eye Diseases
C0086692 BXGD003306 Benign Neoplasm Neoplasms
C0149721 BXGD003349 Left Ventricular Hypertrophy Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0149871 BXGD003375 Deep Vein Thrombosis Cardiovascular Diseases
C0149925 BXGD003387 Small cell carcinoma of lung Neoplasms; Respiratory Tract Diseases
C0151311 BXGD003412 Cranial nerve palsies Nervous System Diseases
C0151491 BXGD003428 Congenital musculoskeletal anomalies Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0151514 BXGD003429 Atrophic condition of skin Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
C0151526 BXGD003432 Premature Birth Female Urogenital Diseases and Pregnancy Complications
C0151636 BXGD003451 Premature ventricular contractions Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0151691 BXGD003460 Decreased HDL cholesterol concentration Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
C0151699 BXGD003461 Intracranial Hemorrhage Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases
C0151786 BXGD003475 Muscle Weakness Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
C0151872 BXGD003493 Prothrombin time increased Hemic and Lymphatic Diseases
C0151878 BXGD003495 Prolonged QT interval Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0151888 BXGD003497 Hyporeflexia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0152013 BXGD003516 Adenocarcinoma of lung (disorder) Neoplasms
C0152025 BXGD003521 Polyneuropathy Nervous System Diseases
C0152421 BXGD003586 Macrotia
C0152438 BXGD003592 Sprengel deformity Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C0153690 BXGD003684 Secondary malignant neoplasm of bone Pathological Conditions, Signs and Symptoms; Neoplasms; Musculoskeletal Diseases
C0158266 BXGD003878 Intervertebral Disc Degeneration Musculoskeletal Diseases
C0162298 BXGD003933 Joint stiffness Musculoskeletal Diseases
C0162834 BXGD003988 Hyperpigmentation Skin and Connective Tissue Diseases
C0178874 BXGD004037 Tumor Progression Pathological Conditions, Signs and Symptoms
C0202239 BXGD004087 Uric acid measurement (procedure)
C0205645 BXGD004097 Adenocarcinoma, Tubular Neoplasms
C0205698 BXGD004109 Undifferentiated carcinoma Neoplasms
C0205713 BXGD004114 Roussy-Levy Syndrome (disorder) Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0205788 BXGD004122 Histiocytoid hemangioma Neoplasms
C0206157 BXGD004165 Myopathies, Nemaline Musculoskeletal Diseases; Nervous System Diseases
C0206602 BXGD004182 Circovirus Infections Infections
C0206650 BXGD004214 Fibroadenoma Neoplasms
C0206664 BXGD004226 Teratocarcinoma Neoplasms
C0206692 BXGD004243 Carcinoma, Lobular Neoplasms; Skin and Connective Tissue Diseases
C0206693 BXGD004244 Medullary carcinoma Neoplasms
C0206698 BXGD004248 Cholangiocarcinoma Neoplasms
C0206711 BXGD004259 Pilomatrixoma Neoplasms
C0220605 BXGD004294 Adult Non-Hodgkin Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0220612 BXGD004296 Childhood Non-Hodgkin Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0220613 BXGD004297 Adult Soft Tissue Sarcoma
C0220645 BXGD004307 Childhood Soft Tissue Sarcoma
C0220989 BXGD004353 Acquired partial lipodystrophy Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
C0221032 BXGD004374 Familial generalized lipodystrophy Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
C0221170 BXGD004400 Muscular stiffness Nervous System Diseases
C0221217 BXGD004408 Neck webbing Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C0221357 BXGD004449 Brachydactyly Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0221365 BXGD004452 Double ureter
C0221629 BXGD004467 Proximal muscle weakness Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
C0231341 BXGD004492 Premature aging syndrome Pathological Conditions, Signs and Symptoms
C0231528 BXGD004496 Myalgia Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
C0231712 BXGD004519 Waddling gait Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0232216 BXGD004537 Ventricular escape rhythm
C0232466 BXGD004543 Feeding difficulties
C0232513 BXGD004553 Premature tooth loss Stomatognathic Diseases
C0232940 BXGD004569 Secondary physiologic amenorrhea Pathological Conditions, Signs and Symptoms
C0234146 BXGD004626 Absent reflex Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0235031 BXGD004714 Neurologic Symptoms Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0235357 BXGD004742 Hypoplasia of teeth Digestive System Diseases; Stomatognathic Diseases
C0235659 BXGD004763 Reduced fetal movement Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications
C0236734 BXGD004823 Caffeine related disorders
C0237849 BXGD004849 Peeling of skin
C0238033 BXGD004861 Carcinoma of Male Breast Neoplasms; Skin and Connective Tissue Diseases
C0238190 BXGD004890 Inclusion Body Myositis (disorder) Musculoskeletal Diseases; Nervous System Diseases
C0238288 BXGD004905 Muscular Dystrophy, Facioscapulohumeral Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C0238462 BXGD004937 Medullary carcinoma of thyroid Neoplasms; Endocrine System Diseases
C0238463 BXGD004938 Papillary thyroid carcinoma Neoplasms; Endocrine System Diseases
C0238621 BXGD004947 Aminoaciduria Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
C0239174 BXGD004969 Late tooth eruption
C0239234 BXGD004974 Low set ears
C0239479 BXGD004982 Round face
C0240479 BXGD005039 Neck muscle weakness Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
C0240538 BXGD005041 Convex nasal ridge
C0240635 BXGD005047 Byzanthine arch palate Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Stomatognathic Diseases
C0240733 BXGD005051 Peroneal muscle weakness
C0240912 BXGD005062 Vertical Talus Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0240953 BXGD005067 Winged scapula
C0241005 BXGD005072 Creatine phosphokinase serum increased
C0241011 BXGD005073 Low serum estradiol levels
C0241267 BXGD005091 Absence of subcutaneous fat
C0241703 BXGD005109 High pitched voice
C0242339 BXGD005150 Dyslipidemias Nutritional and Metabolic Diseases
C0242379 BXGD005157 Malignant neoplasm of lung Neoplasms; Respiratory Tract Diseases
C0242698 BXGD005189 Ventricular Dysfunction, Left Cardiovascular Diseases
C0242787 BXGD005195 Malignant neoplasm of male breast Neoplasms; Skin and Connective Tissue Diseases; Endocrine System Diseases
C0262444 BXGD005244 Abnormality of the dentition Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases
C0263409 BXGD005300 Linear Scleroderma Skin and Connective Tissue Diseases
C0263491 BXGD005315 Pili Torti Skin and Connective Tissue Diseases
C0263498 BXGD005316 Premature canities
C0263505 BXGD005318 Alopecia universalis Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
C0263625 BXGD005332 Subcutaneous calcification Skin and Connective Tissue Diseases
C0264303 BXGD005379 Laryngomalacia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Respiratory Tract Diseases; Otorhinolaryngologic Diseases
C0264789 BXGD005428 Familial cardiomyopathy Cardiovascular Diseases
C0264886 BXGD005432 Conduction disorder of the heart Cardiovascular Diseases
C0264906 BXGD005434 Second degree atrioventricular block Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0265264 BXGD005490 Holt-Oram syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Cardiovascular Diseases
C0265610 BXGD005555 Clinodactyly of fingers Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0265783 BXGD005575 Congenital hypoplasia of lung Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases
C0266009 BXGD005604 Congenital absence of breast Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C0266054 BXGD005615 Premature tooth eruption
C0266200 BXGD005630 Microcolon Digestive System Diseases
C0266786 BXGD005713 Short cord
C0268731 BXGD006029 Renal glomerular disease Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0270254 BXGD006073 Hydrops of placenta Female Urogenital Diseases and Pregnancy Complications
C0270914 BXGD006131 Hereditary Motor and Sensory-Neuropathy Type II Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0270921 BXGD006133 Axonal neuropathy Nervous System Diseases
C0270960 BXGD006141 Congenital myopathy (disorder) Musculoskeletal Diseases; Nervous System Diseases
C0270962 BXGD006142 Multi-core congenital myopathy Musculoskeletal Diseases; Nervous System Diseases
C0271561 BXGD006213 Somatotropin deficiency Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Endocrine System Diseases
C0271623 BXGD006222 Hypogonadotropic hypogonadism Endocrine System Diseases
C0271650 BXGD006227 Impaired glucose tolerance Nutritional and Metabolic Diseases
C0271693 BXGD006238 Acquired generalized lipodystrophy Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Endocrine System Diseases
C0271694 BXGD006239 Familial partial lipodystrophy Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
C0277828 BXGD006480 Late fontanel closure
C0278134 BXGD006498 Absence of sensation Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0278601 BXGD006547 Inflammatory Breast Carcinoma Neoplasms; Skin and Connective Tissue Diseases
C0278838 BXGD006599 Prostate cancer recurrent Neoplasms; Male Urogenital Diseases
C0278878 BXGD006609 Adult Glioblastoma Neoplasms
C0279546 BXGD006633 Adult Undifferentiated Pleomorphic Sarcoma Neoplasms
C0279563 BXGD006637 Lobular carcinoma in situ of breast Neoplasms; Skin and Connective Tissue Diseases
C0279565 BXGD006638 Invasive Lobular Breast Carcinoma Neoplasms; Skin and Connective Tissue Diseases
C0279942 BXGD006700 Metastatic Childhood Soft Tissue Sarcoma
C0280089 BXGD006711 Carcinoid tumor of lung Neoplasms; Respiratory Tract Diseases
C0280100 BXGD006713 Solid Neoplasm Neoplasms
C0280474 BXGD006748 Childhood Glioblastoma Neoplasms
C0282612 BXGD006820 Prostatic Intraepithelial Neoplasias Neoplasms
C0311394 BXGD006884 Difficulty walking Pathological Conditions, Signs and Symptoms
C0332601 BXGD006896 Cushingoid facies Endocrine System Diseases
C0332853 BXGD006901 Anastomosis
C0333068 BXGD006920 Flexion contracture Musculoskeletal Diseases
C0333641 BXGD006961 Atrophic Pathological Conditions, Signs and Symptoms
C0334373 BXGD007051 Intraductal papillary adenocarcinoma with invasion Neoplasms
C0334384 BXGD007053 Infiltrating duct and lobular carcinoma Neoplasms; Skin and Connective Tissue Diseases
C0334463 BXGD007076 Malignant Fibrous Histiocytoma Neoplasms
C0338451 BXGD007176 Frontotemporal dementia Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders
C0338656 BXGD007211 Impaired cognition Mental Disorders
C0340279 BXGD007314 Ventricular hypertrophy Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0340427 BXGD007329 Familial dilated cardiomyopathy Cardiovascular Diseases
C0340489 BXGD007336 Lone atrial fibrillation Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0342257 BXGD007447 Complications of Diabetes Mellitus Endocrine System Diseases
C0342335 BXGD007461 insulin resistance in diabetes Nutritional and Metabolic Diseases
C0342336 BXGD007462 Insulin resistance - type A Nutritional and Metabolic Diseases; Endocrine System Diseases
C0342482 BXGD007486 X-linked Adrenal Hypoplasia Endocrine System Diseases
C0342942 BXGD007583 Generalized obesity Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases
C0344312 BXGD007665 White forelock Skin and Connective Tissue Diseases
C0344424 BXGD007669 Ventricular Arrhythmia by ECG Finding
C0344917 BXGD007708 Left ventricular outflow tract obstruction
C0345392 BXGD007732 Congenital kyphoscoliosis Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0345832 BXGD007742 Neoplasm of small intestine Digestive System Diseases; Neoplasms
C0346169 BXGD007787 Ovarian Cystadenoma Neoplasms
C0349588 BXGD007933 Short stature
C0349782 BXGD007954 Ischemic cardiomyopathy Cardiovascular Diseases
C0349788 BXGD007956 Arrhythmogenic Right Ventricular Dysplasia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C0376358 BXGD007992 Malignant neoplasm of prostate Neoplasms; Male Urogenital Diseases
C0376545 BXGD008002 Hematologic Neoplasms Neoplasms; Hemic and Lymphatic Diseases
C0376634 BXGD008006 Craniofacial Abnormalities Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0392557 BXGD008056 Nuclear cataract Eye Diseases
C0392777 BXGD008068 Poikiloderma Pathological Conditions, Signs and Symptoms
C0398625 BXGD008203 Protein C Deficiency Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
C0400936 BXGD008264 Autoimmune liver disease Digestive System Diseases; Immune System Diseases
C0406585 BXGD008353 Lethal tight skin contracture syndrome (disorder) Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
C0406586 BXGD008354 Wiedemann-Rautenstrauch syndrome Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications
C0409338 BXGD008381 Flexion contracture - elbow
C0409348 BXGD008384 Flexion contracture of proximal interphalangeal joint
C0410174 BXGD008410 Fukuyama Type Congenital Muscular Dystrophy Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases
C0410180 BXGD008412 Eichsfeld type congenital muscular dystrophy Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C0410189 BXGD008413 Muscular Dystrophy, Emery-Dreifuss Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C0410190 BXGD008414 Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder) Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C0410264 BXGD008423 Contracture of tendo achilles
C0423110 BXGD008471 Downward slant of palpebral fissure
C0423112 BXGD008472 Short palpebral fissure
C0423113 BXGD008473 Telecanthus Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0423757 BXGD008504 Thin skin
C0423773 BXGD008506 Scaly skin
C0423808 BXGD008512 Brachyonychia
C0423823 BXGD008515 Thin nails Pathological Conditions, Signs and Symptoms
C0424295 BXGD008524 Hyperactive behavior Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0425957 BXGD008555 Secondary amenorrhea Pathological Conditions, Signs and Symptoms
C0426433 BXGD008566 Pinched nasal tip
C0426790 BXGD008577 Narrow thorax
C0426799 BXGD008578 Congenital hypoplasia of clavicle Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0426807 BXGD008581 Short clavicle
C0426811 BXGD008583 Pseudoarthrosis of clavicle Wounds and Injuries
C0426818 BXGD008586 Thin rib
C0427065 BXGD008604 Distal muscle weakness Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
C0427144 BXGD008607 Toe-walking gait
C0427149 BXGD008608 Gait, Drop Foot Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0428791 BXGD008635 Aortic valve calcification Nutritional and Metabolic Diseases; Cardiovascular Diseases
C0428974 BXGD008642 Supraventricular arrhythmia Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0428975 BXGD008643 Supraventricular Arrhythmia by ECG Finding
C0428977 BXGD008644 Bradycardia Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0431448 BXGD008691 Absent eyebrow Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C0432073 BXGD008719 Defect of skull ossification
C0432103 BXGD008722 Submucous cleft of hard palate Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases
C0432291 BXGD008767 Mandibuloacral dysostosis Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
C0432355 BXGD008780 Hypoplasia of nipple
C0442874 BXGD008814 Neuropathy Nervous System Diseases
C0456070 BXGD008863 Growth delay
C0456132 BXGD008869 Large fontanelle
C0476089 BXGD008977 Endometrial Carcinoma Neoplasms; Female Urogenital Diseases and Pregnancy Complications
C0476403 BXGD008992 Electromyogram abnormal
C0494463 BXGD009029 Alzheimer Disease, Late Onset Nervous System Diseases; Mental Disorders
C0497327 BXGD009061 Dementia Nervous System Diseases; Mental Disorders
C0519097 BXGD009082 Left ventricular aneurysm Cardiovascular Diseases
C0520927 BXGD009124 Decreased fertility
C0520947 BXGD009126 Clumsiness - motor delay Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
C0521858 BXGD009186 Decreased drug resistance
C0524620 BXGD009236 Metabolic Syndrome X Nutritional and Metabolic Diseases
C0541794 BXGD009262 Skeletal muscle atrophy
C0546264 BXGD009330 Congenital Fiber Type Disproportion Musculoskeletal Diseases; Nervous System Diseases
C0549399 BXGD009376 Low density lipoprotein increased Nutritional and Metabolic Diseases
C0549473 BXGD009384 Thyroid carcinoma Neoplasms; Endocrine System Diseases
C0553723 BXGD009416 Squamous cell carcinoma of skin Neoplasms; Skin and Connective Tissue Diseases
C0553730 BXGD009417 Calcium pyrophosphate deposition disease Musculoskeletal Diseases
C0557874 BXGD009444 Global developmental delay
C0560346 BXGD009475 Difficulty running Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0566620 BXGD009490 Nasal voice
C0566693 BXGD009491 Large placenta
C0566694 BXGD009492 Small placenta
C0575081 BXGD009512 Gait abnormality Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0575158 BXGD009515 Kyphoscoliosis deformity of spine Musculoskeletal Diseases
C0575535 BXGD009520 Thin clavicle
C0578038 BXGD009542 Thin lips
C0585442 BXGD009593 Osteosarcoma of bone Neoplasms
C0595939 BXGD009629 Stillbirth Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications
C0596263 BXGD009639 Carcinogenesis Pathological Conditions, Signs and Symptoms; Neoplasms
C0598589 BXGD009667 Inherited neuropathies Nervous System Diseases
C0600033 BXGD009682 Acquired Kyphoscoliosis Musculoskeletal Diseases
C0600139 BXGD009695 Prostate carcinoma Neoplasms; Male Urogenital Diseases
C0678222 BXGD009749 Breast Carcinoma Neoplasms; Skin and Connective Tissue Diseases
C0684249 BXGD009790 Carcinoma of lung Neoplasms; Respiratory Tract Diseases
C0686353 BXGD009833 Muscular Dystrophies, Limb-Girdle Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System 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
C0699790 BXGD009866 Colon Carcinoma Digestive System Diseases; Neoplasms
C0699791 BXGD009867 Stomach Carcinoma Digestive System Diseases; Neoplasms
C0700095 BXGD009875 Central neuroblastoma Neoplasms; Nervous System Diseases
C0741899 BXGD010042 Poorly differentiated carcinoma
C0741916 BXGD010044 Cardiac defects
C0741923 BXGD010045 cardiac event
C0747102 BXGD010159 Ovarian failure Endocrine System Diseases
C0748505 BXGD010198 Sarcoma, metastatic Neoplasms
C0751337 BXGD010393 X-Linked Emery-Dreifuss Muscular Dystrophy Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C0751606 BXGD010523 Adult Acute Lymphocytic Leukemia
C0751674 BXGD010547 Lymphangioleiomyomatosis Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0751713 BXGD010564 Inclusion Body Myopathy, Sporadic Musculoskeletal Diseases; Nervous System Diseases
C0751778 BXGD010587 Myoclonic Epilepsies, Progressive Nervous System Diseases
C0751785 BXGD010594 Unverricht-Lundborg Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0751951 BXGD010648 Central Core Myopathy (disorder) Musculoskeletal Diseases; Nervous System Diseases
C0796031 BXGD010783 Malouf syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases; Cardiovascular Diseases
C0796083 BXGD010795 Najjar syndrome Cardiovascular Diseases
C0812413 BXGD010847 Malignant Pleural Mesothelioma Neoplasms; Respiratory Tract Diseases
C0836924 BXGD010864 Thrombocytosis Hemic and Lymphatic Diseases
C0848558 BXGD010882 Hypospadias Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0853087 BXGD010964 Nail abnormality Pathological Conditions, Signs and Symptoms
C0853879 BXGD010982 Invasive carcinoma of breast Neoplasms; Skin and Connective Tissue Diseases
C0854110 BXGD011000 Insulin-resistant diabetes mellitus Nutritional and Metabolic Diseases; Endocrine System Diseases
C0855329 BXGD011084 Electrocardiogram change
C0856169 BXGD011096 Endothelial dysfunction
C0856742 BXGD011111 Post MI Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0856747 BXGD011112 Aneurysm of ascending aorta Respiratory Tract Diseases; Cardiovascular Diseases
C0856863 BXGD011122 Broad-based gait
C0857379 BXGD011148 Abnormality of the pinna
C0860439 BXGD011224 Mottled pigmentation Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
C0870082 BXGD011309 Hyperkeratosis Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
C0872084 BXGD011319 Sarcopenia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0878544 BXGD011368 Cardiomyopathies Cardiovascular Diseases
C0917713 BXGD011404 Becker Muscular Dystrophy Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C0917990 BXGD011424 Acro-Osteolysis Musculoskeletal Diseases
C0919267 BXGD011426 ovarian neoplasm Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
C0919718 BXGD011437 Calcification of mitral valve
C0948896 BXGD011563 Primary hypogonadism Endocrine System Diseases
C0949658 BXGD011582 Cardiomyopathy, Hypertrophic, Familial Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C0949664 BXGD011583 Tauopathies Nervous System Diseases
C1096616 BXGD011635 Contralateral breast cancer
C1112705 BXGD011681 Nuclear non-senile cataract Eye Diseases
C1134719 BXGD011688 Invasive Ductal Breast Carcinoma Neoplasms; Skin and Connective Tissue Diseases
C1136321 BXGD011716 HIV-Associated Lipodystrophy Syndrome Nutritional and Metabolic Diseases; Infections; Skin and Connective Tissue Diseases; Immune System Diseases
C1136382 BXGD011717 Sclerocystic Ovaries Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
C1140680 BXGD011718 Malignant neoplasm of ovary Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
C1168327 BXGD011787 High-Grade Prostatic Intraepithelial Neoplasia Neoplasms; Male Urogenital Diseases
C1168330 BXGD011790 Non-ischemic dilated cardiomyopathy
C1176475 BXGD011798 Ductal Carcinoma Neoplasms
C1184923 BXGD011800 Lumbar hyperlordosis Musculoskeletal Diseases
C1261473 BXGD011855 Sarcoma Neoplasms
C1263846 BXGD011897 Attention deficit hyperactivity disorder Mental Disorders
C1263857 BXGD011900 Peripheral axonal neuropathy Nervous System Diseases
C1269955 BXGD012005 Tumor Cell Invasion
C1277187 BXGD012109 Left ventricular systolic dysfunction Cardiovascular Diseases
C1280433 BXGD012125 Lipoatrophy Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
C1285162 BXGD012167 Degenerative disorder Pathological Conditions, Signs and Symptoms
C1292769 BXGD012230 Precursor B-cell lymphoblastic leukemia Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C1298820 BXGD012252 Aneurysm of aortic root Cardiovascular Diseases
C1301937 BXGD012300 Talipes Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C1306459 BXGD012361 Primary malignant neoplasm Neoplasms
C1306460 BXGD012362 Primary malignant neoplasm of lung Neoplasms; Respiratory Tract Diseases
C1306837 BXGD012377 Papillary Renal Cell Carcinoma Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C1328407 BXGD012465 Hip Dysplasia Musculoskeletal Diseases; Wounds and Injuries
C1328504 BXGD012469 Hormone refractory prostate cancer Neoplasms; Male Urogenital Diseases
C1332201 BXGD012502 Adult Diffuse Large B-Cell Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C1332206 BXGD012504 Adult Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C1332977 BXGD012569 Childhood Leukemia Neoplasms
C1332979 BXGD012571 Childhood Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C1332986 BXGD012574 Childhood Osteosarcoma Neoplasms
C1333064 BXGD012587 Classical Hodgkin's Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C1334274 BXGD012695 Invasive Carcinoma Neoplasms
C1334708 BXGD012732 Metaplastic carcinoma of breast
C1384666 BXGD012948 hearing impairment Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
C1389113 BXGD012965 Generalized amyotrophy
C1389118 BXGD012966 Peroneal muscle atrophy
C1399793 BXGD013007 skin fold (abnormality)
C1408174 BXGD013034 Hypertrophic neuropathy of infancy
C1408182 BXGD013035 Hereditary motor and sensory neuropathy, types I-IV
C1449563 BXGD013086 Cardiomyopathy, Familial Idiopathic Cardiovascular Diseases
C1450051 BXGD013101 Autosomal Recessive Emery-Dreifuss Muscular Dystrophy Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C1456873 BXGD013129 alpha^+^ Thalassemia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
C1458155 BXGD013136 Mammary Neoplasms Neoplasms; Skin and Connective Tissue Diseases
C1510586 BXGD013176 Autism Spectrum Disorders Mental Disorders
C1527349 BXGD013277 Ductal Breast Carcinoma Neoplasms
C1527383 BXGD013282 Morphea Skin and Connective Tissue Diseases
C1533847 BXGD013318 Disorder of skeletal muscle Musculoskeletal Diseases; Nervous System Diseases
C1611743 BXGD013456 Familial (FPAH)
C1621958 BXGD013468 Glioblastoma Multiforme Neoplasms
C1698196 BXGD013513 Muscle Weakness Upper Limb Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
C1706827 BXGD013578 Apocrine Carcinoma
C1708566 BXGD013607 Invasive Prostate Carcinoma
C1720824 BXGD013686 Sudden Cardiac Arrest Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C1720859 BXGD013688 Familial Partial Lipodystrophy, Type 1 Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
C1720860 BXGD013689 Familial Partial Lipodystrophy, Type 2 Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
C1720861 BXGD013690 Familial Partial Lipodystrophy, Type 3 Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
C1737329 BXGD013728 Dysmorphism Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C1832446 BXGD013844 Sparse eyebrow
C1832931 BXGD013885 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 2 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C1833325 BXGD013913 Thin bony cortex
C1833762 BXGD013945 Decreased calvarial ossification
C1834405 BXGD013970 Nail dysplasia Pathological Conditions, Signs and Symptoms
C1834481 BXGD013975 CARDIOMYOPATHY, DILATED, 1S Cardiovascular Diseases
C1834653 BXGD013983 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1B (disorder) Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C1834674 BXGD013987 BETHLEM MYOPATHY 1 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C1834696 BXGD013989 Hyporeflexia of lower limbs
C1835380 BXGD014023 Labial pseudohypertrophy
C1835384 BXGD014024 Loss of truncal subcutaneous adipose tissue
C1835389 BXGD014025 Increased intramuscular fat
C1835390 BXGD014026 Increased intraabdominal fat
C1836038 BXGD014073 Poor head control Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
C1836451 BXGD014118 Distal lower limb amyotrophy
C1836646 BXGD014141 Dermal translucency
C1836767 BXGD014159 Proximal lower limb amyotrophy
C1836906 BXGD014177 Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C1837260 BXGD014214 Prominent forehead
C1837463 BXGD014235 Narrow face
C1837757 BXGD014264 Progressive clavicular acroosteolysis Musculoskeletal Diseases
C1837758 BXGD014265 Bird-like facies
C1837761 BXGD014266 Narrow nasal ridge
C1837764 BXGD014268 Loss of subcutaneous adipose tissue in limbs
C1837770 BXGD014270 Sparse hair
C1837785 BXGD014271 Prominent superficial veins
C1837792 BXGD014272 Insulin-resistant diabetes mellitus at puberty
C1837802 BXGD014275 Decreased serum leptin
C1838539 BXGD014318 CARDIOMYOPATHY, FAMILIAL, WITH CONDUCTION DISTURBANCE Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C1839630 BXGD014391 Severe muscular hypotonia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C1839653 BXGD014392 Decreased cervical spine flexion due to contractures of posterior cervical muscles
C1839780 BXGD014405 FRAGILE X TREMOR/ATAXIA SYNDROME Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C1839829 BXGD014413 Short distal phalanx of finger
C1842552 BXGD014523 Limb-girdle muscle atrophy
C1843005 BXGD014548 Absent eyelashes
C1843057 BXGD014552 Calf muscle hypertrophy
C1843108 BXGD014556 Short palm
C1843300 BXGD014572 Sparse eyelashes
C1843392 BXGD014582 Death in childhood
C1843697 BXGD014603 Axial muscle weakness Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
C1844618 BXGD014653 Aplasia/Hypoplastia of the eccrine sweat glands
C1846223 BXGD014792 Adrenal hypoplasia
C1846228 BXGD014793 Absence of pubertal development
C1846438 BXGD014816 Hypoplastic facial bones
C1847584 BXGD014876 Distal sensory impairment Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C1847835 BXGD014892 VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding) Skin and Connective Tissue Diseases
C1847906 BXGD014897 Onion bulb formation
C1848486 BXGD014929 Premature arteriosclerosis Cardiovascular Diseases
C1848736 BXGD014970 Distal amyotrophy
C1848760 BXGD014972 Increased anterioposterior diameter of thorax
C1848769 BXGD014973 Overtubulated long bones
C1848771 BXGD014974 Prominent superficial blood vessels Skin and Connective Tissue Diseases
C1848773 BXGD014975 Epidermal hyperkeratosis
C1849039 BXGD014999 Metaphyseal widening
C1849211 BXGD015023 Generalized hirsutism Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
C1849300 BXGD015032 Widely patent fontanelles and sutures
C1849367 BXGD015046 Nasal bridge wide
C1849547 BXGD015066 Osteolytic defects of the distal phalanges of the hand Musculoskeletal Diseases
C1849618 BXGD015072 Accelerated atherosclerosis Cardiovascular Diseases
C1850663 BXGD015169 Muscle hypertrophy of the lower extremities
C1850830 BXGD015181 Exercise-induced myalgia Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
C1851792 BXGD015234 Aplasia/Hypoplasia of the earlobes
C1851808 BXGD015237 Premature delivery because of cervical insufficiency or membrane fragility Female Urogenital Diseases and Pregnancy Complications
C1852502 BXGD015286 CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT Musculoskeletal Diseases; Stomatognathic Diseases
C1853242 BXGD015322 Midface retrusion
C1853932 BXGD015366 Rimmed vacuoles on biopsy
C1854154 BXGD015385 Charcot-Marie-Tooth disease, Type 2B1 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C1854301 BXGD015391 Motor delay Mental Disorders
C1854494 BXGD015409 Slow progression
C1855665 BXGD015524 Ovoid vertebral bodies
C1856542 BXGD015615 Prominent scalp veins
C1856872 BXGD015647 Down-sloping shoulders
C1856963 BXGD015662 Fragile nails Pathological Conditions, Signs and Symptoms
C1857042 BXGD015669 Sparse scalp hair
C1857108 BXGD015677 Limitation of joint mobility
C1857657 BXGD015732 Reduced subcutaneous adipose tissue
C1857665 BXGD015734 Aplastic clavicle
C1857710 BXGD015743 Progeroid facial appearance
C1857829 BXGD015754 Heart-hand syndrome, Slovenian type Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Cardiovascular Diseases
C1858025 BXGD015760 Spinal rigidity
C1858085 BXGD015770 Malar flattening
C1858120 BXGD015774 Generalized hypotonia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C1858127 BXGD015775 Limb-girdle muscle weakness Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
C1858285 BXGD015781 Decreased number of peripheral myelinated nerve fibers
C1858430 BXGD015792 Death in infancy
C1858729 BXGD015825 Decreased motor nerve conduction velocity
C1859442 BXGD015890 Minimal subcutaneous fat
C1859592 BXGD015912 ATRICHIA WITH PAPULAR LESIONS Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
C1859778 BXGD015931 Postnatal growth retardation
C1861403 BXGD016045 Variable expressivity
C1861922 BXGD016094 CAMPOMELIC DYSPLASIA Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C1862096 BXGD016101 Aplasia of the middle phalanx of the hand
C1862475 BXGD016132 Abnormality of retinal pigmentation
C1862863 BXGD016138 Sparse body hair
C1864954 BXGD016278 Fasting hyperinsulinemia Nutritional and Metabolic Diseases
C1866010 BXGD016360 Proximal muscle weakness in lower limbs
C1866012 BXGD016361 Proximal muscle weakness in upper limbs
C1866013 BXGD016362 Proximal upper limb amyotrophy
C1866141 BXGD016379 Foot dorsiflexor weakness
C1866231 BXGD016388 Full cheeks
C1866934 BXGD016427 Reduced tendon reflexes Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C1867006 BXGD016434 Restricted neck movement due to contractures
C1867114 BXGD016439 Craniofacial disproportion
C1867743 BXGD016470 Premature coronary artery atherosclerosis Cardiovascular Diseases
C1868938 BXGD016542 End stage cardiac failure
C1883529 BXGD016597 Ventricular Arrhythmia, CTCAE 3.0
C1956346 BXGD016627 Coronary Artery Disease Cardiovascular Diseases
C1960469 BXGD016664 Left ventricular noncompaction Cardiovascular Diseases
C1961102 BXGD016673 Precursor Cell Lymphoblastic Leukemia Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C1968790 BXGD016736 Axonal degeneration/regeneration
C1969913 BXGD016800 Generalized hyperkeratosis
C2063326 BXGD016902 Right ventricular cardiomyopathy Cardiovascular Diseases
C2145472 BXGD016931 Urothelial Carcinoma Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C2239176 BXGD016965 Liver carcinoma Digestive System Diseases; Neoplasms
C2265792 BXGD017012 Skeletal muscle hypertrophy
C2266788 BXGD017014 Trichilemmal cyst Neoplasms
C2267233 BXGD017017 Neonatal Hypotonia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C2316810 BXGD017030 Chronic kidney disease stage 5 Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C2347747 BXGD017040 Adult Classical Hodgkin Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C2362324 BXGD017091 Pediatric Obesity Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases
C2363741 BXGD017100 HIV-1 infection
C2675074 BXGD017269 Enlarged peripheral nerve
C2678065 BXGD017398 Myofibrillar Myopathy Musculoskeletal Diseases; Nervous System Diseases
C2711227 BXGD017478 Steatohepatitis Digestive System Diseases
C2748542 BXGD017596 CARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder) Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C2750035 BXGD017641 Emery-Dreifuss Muscular Dystrophy 3 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C2750285 BXGD017655 Progeria Syndrome, Childhood-Onset Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
C2750785 BXGD017677 MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED (disorder) Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C2827469 BXGD017798 Coronary Microvascular Disease
C2875300 BXGD017836 Peroneal muscular atrophy (axonal type) (hypertrophic type)
C2875316 BXGD017838 Myotubular (centronuclear) myopathy
C2919142 BXGD017867 Short Stature, CTCAE
C2931375 BXGD018011 Temporomandibular ankylosis Musculoskeletal Diseases; Stomatognathic Diseases
C2931687 BXGD018048 Dysferlinopathy Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C2931822 BXGD018068 Nasopharyngeal carcinoma Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases
C2936331 BXGD018106 Sarcoglycanopathies Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Respiratory Tract Diseases; Nervous System Diseases; Cardiovascular Diseases
C2939419 BXGD018178 Secondary Neoplasm Pathological Conditions, Signs and Symptoms; Neoplasms
C2945759 BXGD018189 aggressive cancer
C2986665 BXGD018237 Early-Stage Breast Carcinoma Neoplasms; Skin and Connective Tissue Diseases
C3148763 BXGD018270 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1E Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C3266164 BXGD018599 Dropped head syndrome
C3276815 BXGD018696 Stiff skin
C3279575 BXGD018764 Reticulated skin pigmentation
C3279947 BXGD018789 NAIL DISORDER, NONSYNDROMIC CONGENITAL, 9
C3280303 BXGD018820 Abnormal hair whorl
C3469521 BXGD018910 FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder) Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
C3469529 BXGD018916 FANCONI ANEMIA, COMPLEMENTATION GROUP M
C3494422 BXGD018966 Retrognathia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases
C3539878 BXGD019087 Triple Negative Breast Neoplasms Neoplasms; Skin and Connective Tissue Diseases
C3551431 BXGD019147 Sparse or absent eyelashes
C3553764 BXGD019187 Joint hyperflexibility
C3714619 BXGD019418 Insulin resistance syndrome Nutritional and Metabolic Diseases
C3714796 BXGD019434 Isolated somatotropin deficiency
C3806467 BXGD019513 Respiratory insufficiency due to muscle weakness Respiratory Tract Diseases
C3810018 BXGD019629 Bilateral coxa valga Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases
C3854222 BXGD019826 Human immunodeficiency virus (HIV) II infection category B1
C3887524 BXGD019892 Skin Erosion Skin and Connective Tissue Diseases
C3888631 BXGD019983 Monogenic diabetes Nutritional and Metabolic Diseases; Endocrine System Diseases
C3898127 BXGD020061 Non-Metastatic Childhood Soft Tissue Sarcoma
C3899638 BXGD020085 Childhood Undifferentiated Pleomorphic Sarcoma Neoplasms
C4011556 BXGD020113 Abnormal eyebrow morphology
C4015465 BXGD020208 Thoracic kyphoscoliosis
C4016241 BXGD020295 HUTCHINSON-GILFORD PROGERIA SYNDROME, ATYPICAL
C4020957 BXGD020507 Abnormal trabecular bone morphology
C4021573 BXGD020680 Patchy hypo- and hyperpigmentation
C4021642 BXGD020715 Abnormality of the Achilles tendon Musculoskeletal Diseases
C4021654 BXGD020722 Precocious atherosclerosis Cardiovascular Diseases
C4021684 BXGD020729 Sclerosis of hand bone Musculoskeletal Diseases
C4021726 BXGD020735 EMG: myopathic abnormalities Musculoskeletal Diseases; Nervous System Diseases
C4021776 BXGD020772 Abnormality of the voice
C4021779 BXGD020774 Abnormality of the calf musculature
C4021790 BXGD020782 Abnormality of the skeletal system
C4021956 BXGD020839 Aplasia/Hypoplasia of the eyebrow
C4021998 BXGD020862 Lack of skin elasticity
C4022001 BXGD020863 Abnormality of the cerebral vasculature
C4022018 BXGD020872 Telangiectasia of the skin Cardiovascular Diseases
C4022125 BXGD020882 Aplasia of the phalanges of the 3rd toe
C4022583 BXGD020924 Fatiguable weakness of proximal limb muscles
C4022628 BXGD020940 Absent muscle fiber emerin
C4023051 BXGD021084 Abnormality of skeletal muscle fiber size
C4023180 BXGD021139 Type 1 muscle fiber atrophy
C4023222 BXGD021148 Abnormal electrophysiology of sinoatrial node origin Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C4023402 BXGD021178 Regional abnormality of skin
C4023577 BXGD021220 Abnormality of the intrahepatic bile duct
C4023965 BXGD021281 Structural foot deformity Musculoskeletal Diseases
C4024159 BXGD021292 Aplasia/Hypoplasia involving the nose
C4024589 BXGD021330 Aplasia/Hypoplasia of the mandible
C4024615 BXGD021345 Adipose tissue loss
C4024957 BXGD021500 Proximal spinal muscular atrophy Nervous System Diseases
C4024993 BXGD021516 Aplasia/Hypoplasia of the clavicles
C4025078 BXGD021545 Tapering pointed ends of distal finger phalanges
C4025213 BXGD021594 Abnormality of complement system
C4025244 BXGD021603 Abnormal atrioventricular conduction
C4025270 BXGD021613 Arteriosclerosis of small cerebral arteries Cardiovascular Diseases
C4025272 BXGD021615 Peripheral arterial stenosis
C4025339 BXGD021648 Abnormality of circulating leptin level
C4025619 BXGD021698 Peripheral axonal atrophy
C4025739 BXGD021768 Acroosteolysis of distal phalanges (feet)
C4025850 BXGD021828 Increased adipose tissue around the neck
C4025868 BXGD021837 Increased facial adipose tissue
C4025886 BXGD021846 Severe periodontitis Stomatognathic Diseases
C4049702 BXGD021948 Focal Segmental Glomerulosclerosis, Not Otherwise Specified Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C4073127 BXGD022042 Decreased adiponectin level
C4073137 BXGD022045 Decreased serum testosterone level
C4086165 BXGD022126 Childhood Neuroblastoma Neoplasms
C4229131 BXGD022293 Distal acroosteolysis
C4275075 BXGD022363 Atypical Werner syndrome Pathological Conditions, Signs and Symptoms
C4280686 BXGD022384 Proximal upper limb muscle hypertrophy
C4282407 BXGD022423 Sparse and thin eyebrow
C4316789 BXGD022698 Partial lipodystrophy Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
C4317112 BXGD022726 Generalized Lipodystrophy Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
C4476724 BXGD022854 Abnormal cellular phenotype
C4521256 BXGD023058 Glomerulopathy Assessment
C4523846 BXGD023079 MSI-high
C4531142 BXGD023193 Abnormal lymphocyte physiology
C4551472 BXGD023303 Hypertrophic obstructive cardiomyopathy Cardiovascular Diseases
C4551485 BXGD023312 Clinodactyly
C4551514 BXGD023331 Hemophagocytic Lymphohistiocytosis, Familial, 1 Hemic and Lymphatic Diseases
C4551647 BXGD023381 Long QT Syndrome 1 Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C4551680 BXGD023387 Generalized osteoporosis Nutritional and Metabolic Diseases; Musculoskeletal Diseases
C4551687 BXGD023392 Sarcoma of soft tissue Neoplasms
C4551915 BXGD023441 Gait Disturbance, CTCAE
C4552766 BXGD023523 Miscarriage Female Urogenital Diseases and Pregnancy Complications
C4553764 BXGD023550 Ventricular Arrhythmia, CTCAE 5.0
C4553962 BXGD023553 Hyperkeratosis, CTCAE
C4721208 BXGD023733 Metastatic castration-resistant prostate cancer
C4721411 BXGD023735 Osteolysis Musculoskeletal Diseases
C4721453 BXGD023744 Peripheral Nervous System Diseases Nervous System Diseases
C4721532 BXGD023752 Lymphoma, Non-Hodgkin, Familial Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C4721579 BXGD023759 Secondary malignant neoplasm of colon and/or rectum Digestive System Diseases; Neoplasms
C4721610 BXGD023760 Carcinoma, Ovarian Epithelial Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
C4721806 BXGD023772 Carcinoma, Basal Cell Neoplasms
C4722085 BXGD023788 Malignant neoplasm of colon and/or rectum
C4722518 BXGD023806 Triple-Negative Breast Carcinoma Neoplasms; Skin and Connective Tissue Diseases
C4724394 BXGD023815 Metastatic Soft Tissue Sarcoma
C4750858 BXGD024078 LMNA-related cardiocutaneous progeria syndrome Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
Target protein-related  compounds
Compounds
BXGC Id Compound Name Strcuture Molecular Weight
BXGC0000099 3,4-Dihydroxyphenylacetic acid 168.15
BXGC0000130 Estradiol 272.38
BXGC0000164 Oxoglaucine 351.35
BXGC0000194 Sanguinarine 332.33
BXGC0000202 Papaverine 339.39
BXGC0000242 L-Canavanine 176.17
BXGC0000244 S-Carboxymethyl-L-cysteine 179.19
BXGC0000284 alpha-Tocopherol 430.71
BXGC0000288 L-Proline 115.13
BXGC0000332 Fisetin 286.24
BXGC0000340 Kaempferol 286.24
BXGC0000368 Gallic acid 170.12
BXGC0000369 Methyl gallate 184.15
BXGC0000430 Gossypol 518.55
BXGC0000433 Triacetin 218.2
BXGC0000436 Glycerol 92.09
BXGC0000439 Chloroform 119.38
BXGC0000445 Pentane 72.15
BXGC0000530 Hydroquinone 110.11
BXGC0000573 Dantron 240.21
BXGC0000663 Papain 206.28
BXGC0000759 Arabinan 243.22
BXGC0000895 5-Hydroxyindole-3-acetic acid 191.18
BXGC0000952 6-Oxocamphor 457.91
BXGC0000988 3' 5'-cyclic AMP 329.21
BXGC0001002 1,2-Benzenediol 110.11
BXGC0001076 4-Hydroxyderricin 338.4
BXGC0001079 Xanthoangelol 392.49
BXGC0001273 Hippuric acid 179.17
BXGC0001325 Progesterone 314.46
BXGC0001380 Succinic acid 118.09
BXGC0001411 D-Mannitol 182.17
BXGC0001451 (S)-Laudanosine 357.44
BXGC0001544 Harmaline 214.26
BXGC0001589 Arecoline 155.19
BXGC0001623 L-Tryptophan 204.23
BXGC0001746 Theaflavin 3,3'-digallate 868.7
BXGC0001767 (E)-Resveratrol 228.25
BXGC0001789 Silibinin 482.44
BXGC0001857 Caffeic acid 180.16
BXGC0001899 Daidzein 254.24
BXGC0001940 Daphnetin 178.14
BXGC0001994 Hyperin 464.38
BXGC0001995 Maltol 126.11
BXGC0002043 Acacetin 284.26
BXGC0002052 Aesculetin 178.14
BXGC0002069 Anethole 148.2
BXGC0002071 Apigenin 270.24
BXGC0002094 Rhamnetin 316.26
BXGC0002279 Cetyl alcohol 242.44
BXGC0002336 Glycerol trioctanoate 470.68
BXGC0002374 Taurine 125.15
BXGC0002400 Ethyl acetate 88.11
BXGC0002439 4-Oxopentanoic acid 116.12
BXGC0002468 Octanoic acid 144.21
BXGC0002735 Carotene 536.89
BXGC0002789 Isoimperatorin 270.28
BXGC0002820 alpha-Amino-beta-hydroxybutyric acid 119.12
BXGC0002906 Caffeic acid ester 284.31
BXGC0002916 Melatonin 232.28
BXGC0002958 Dioctyl phthalate 390.56
BXGC0002971 alpha-Lipoic acid 206.33
BXGC0003066 Phenols 199.27
BXGC0003218 Foluene 92.14
BXGC0003249 5-Hexyl-2-methylpyridine 270.37
BXGC0003364 Cerebroside 299.49
BXGC0003392 Isoxanthopterin 179.14
BXGC0003464 Satiomem 290.79
BXGC0003466 Calamene 301.69
BXGC0003502 Phenylhydrazine 108.14
BXGC0003610 5-Hydroxy-L-tryptophan 220.22
BXGC0003627 alpha-Linoleic acid 280.45
BXGC0003678 Sphondin 216.19
BXGC0003690 Glucokinin 764.94
BXGC0003707 Estrogen 268.36
BXGC0003765 Psidiolic acid 129.11
BXGC0003852 Nigrin B 506.47
BXGC0003949 Thymunic acid 150.22
BXGC0003956 Fenugrin E 178.19
BXGC0004132 Zosimin 328.36
BXGC0004266 2-Propanol 60.1
BXGC0004274 1,1-Diethoxyethane 118.17
BXGC0004276 Acetamide 59.07
BXGC0004278 Acetone 58.08
BXGC0004279 Acrylic acid 72.06
BXGC0004284 Hexanedioic acid 146.14
BXGC0004365 Propyl benzoate 164.2
BXGC0004378 3-Hydroxyflavone 238.24
BXGC0004497 3-O-Acetylepisamarcandin 442.54
BXGC0004556 1,2,3-Benzenetriol 126.11
BXGC0004559 1,3-Benzenediol 110.11
BXGC0004563 Benzoyl peroxide 242.23
BXGC0004576 2-tert-Butyl-1,4-benzenediol 166.22
BXGC0004577 4-tert-Butylphenol 150.22
BXGC0004587 (E)-3-Phenyl-2-propenal 132.16
BXGC0004592 p-Tolyl acetate 150.17
BXGC0004665 4-Aminobutyric acid 103.12
BXGC0004738 Myo-Inositol 180.16
BXGC0004965 Rhein 284.22
BXGC0005428 Graveoline 279.29
BXGC0005458 Oxopurpureine 381.38
BXGC0005502 Coumestrol 268.22
BXGC0005624 Genistein 270.24
BXGC0005638 Undecylenic acid 184.28
BXGC0005659 Arachidonic acid 304.47
BXGC0005683 Quercetin 302.24
BXGC0005702 2H-1-Benzopyran-2-one 146.15
BXGC0005857 Isoginkgetin 566.51
BXGC0005865 L-Selenomethionine 196.11
BXGC0005881 Urea 60.06
BXGC0005894 Azelaic acid 188.22
BXGC0005917 Genistin 432.38
BXGC0005919 Biochanin A 284.27
BXGC0005982 Curcumin 368.38
BXGC0006057 (Z)-Resveratrol 228.25
BXGC0006105 Methyl salicylate 152.15
BXGC0006107 alpha-Linolenic acid 278.43
BXGC0006156 Dicoumarol 336.3
BXGC0006186 L-Aspartic acid 133.1
BXGC0006193 Ellagic acid 302.19
BXGC0006336 1-Octadecanol 270.49
BXGC0006362 Estrone 270.37
BXGC0006389 Rotenone 394.42
BXGC0006604 Perillic acid 166.22
BXGC0006617 Coenzyme Q 863.34
BXGC0006635 Luteolin 286.24
BXGC0006795 Limonene 136.24
BXGC0007029 Emodin 270.24
BXGC0007467 alpha-Terpineol 154.25
BXGC0007471 3H-1,2-Dithiole-3-thione 134.24
BXGC0007499 Boric acid (H3BO3) 61.83
BXGC0007533 Biotin 244.31
BXGC0007550 Lycopene 536.89
BXGC0007601 1,8-Cineole 154.25
BXGC0008129 Carbon disulfide 76.14
BXGC0008184 Phloretin 274.27
BXGC0008198 7-Isopropyl-1,4-dimethylazulene 198.3
BXGC0008707 Isoliquiritigenin 256.25
BXGC0008937 Demethylnobiletin 388.37
BXGC0009194 Quercetin 3-glucuronide 478.36
BXGC0009332 Pelanin 356.5
BXGC0010354 Cytokinin B 225.25
BXGC0011627 Glycyrrhetic acid 470.69
BXGC0012377 Nagilactone B 364.15
BXGC0013509 Cathine 151.1
BXGC0013612 Etofylline 224.09
BXGC0013854 Histamine 111.08
BXGC0014545 Hydrocodone 299.15
BXGC0014695 Loratadine 382.14
BXGC0014944 Chelidonine (+) 353.13
BXGC0015075 Benzyl Cinnamate 238.1
BXGC0015208 Getiacaulein 288.06
BXGC0015236 (6R)-6-[(5R)-6-Methyl-7,8-Dihydro-5H-[1,3]Dioxolo[4,5-G]Isoquinolin-5-Yl]-6H-Furo[3,4-G][1,3]Benzodioxol-8-One 367.11
BXGC0015594 4-Nonylphenol 220.18
BXGC0015879 Chlorhexidine 504.2
BXGC0016247 3,5-Dihydroxy-2-Phenylchromen-4-One 254.06
BXGC0016470 Camptothecin 348.11
BXGC0016681 Hispidin 246.05
BXGC0016747 Camphor 152.12
BXGC0016788 D-Valine 117.08
BXGC0016866 Rhetsinine 319.13
BXGC0016886 Papaverine Hydrochloride 339.15
BXGC0016891 Nortriptyline 263.17
BXGC0016973 Guvacine Hydrochloride 127.06
BXGC0016978 (4R)-4-Hydroxy-4-Methyloxan-2-One 130.06
BXGC0017100 1,2-Dichlorobenzene 145.97
BXGC0017232 Dipyrithione 252
BXGC0017596 Jatrorrhizine 338.14
BXGC0017628 canadine 339.15
BXGC0017757 Androstenedione 286.19
BXGC0018063 Alprenolol 249.17
BXGC0018403 Hydroxyprogesterone 330.22
BXGC0019091 D-Tryptophan 204.09
BXGC0019164 Raloxifene 473.17
BXGC0019352 Sparteine 234.21
BXGC0019377 Cumingianoside A 738.46
BXGC0020680 Mandelic Acid 152.05
BXGC0020694 Betonicine 159.09
BXGC0020737 Protoapigenone 286.05
BXGC0020800 Testosterone 288.21
BXGC0020835 5-(6-Aminopurin-9-Yl)-2-(Hydroxymethyl)Oxolan-3-Ol 251.1
BXGC0020943 D-Leucine 131.09
BXGC0021212 Palmitine 352.15
BXGC0021478 Lipoic Acid 206.04
BXGC0021666 dicentrine 339.15
BXGC0021716 (R)-Verapamil 454.28
BXGC0021893 Norepinephrine 169.07
BXGC0022321 Squalane 422.49
BXGC0022544 Digoxin 780.43
BXGC0022806 1-(5-Thiophen-2-Ylthiophen-2-Yl)Ethanone 208
BXGC0023039 (10-Acetyloxy-8,8-Dimethyl-2-Oxo-9,10-Dihydropyrano[2,3-F]Chromen-9-Yl) 3-Methylbutanoate 388.15
BXGC0023180 (1S,5R)-8-Methyl-8-Azabicyclo[3.2.1]Octan-3-Ol 141.12
BXGC0023542 Erysolin 193.02
BXGC0023633 Kamebanin 334.21
BXGC0023771 1,4-Dichlorobenzene 145.97
BXGC0023872 Adenine 135.05
BXGC0023917 Cearoin 244.07
BXGC0024256 (8S,10R,11S,13S,14S,17S)-11-Hydroxy-17-(2-Hydroxyacetyl)-10,13-Dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-Dodecahydrocyclopenta[A]Phenanthren-3-One 346.21
BXGC0024428 3-(1H-Benzimidazol-2-Yl)-7-(Diethylamino)Chromen-2-One 333.15
BXGC0024537 E309 402.35
BXGC0024561 (1S)-1-[(3,4-Dimethoxyphenyl)Methyl]-6,7-Dimethoxy-2-Methyl-3,4-Dihydro-1H-Isoquinoline 357.19
BXGC0024863 (2R)-5-Amino-2-Azaniumyl-5-Oxopentanoate 146.07
BXGC0024988 Nifedipine 346.12
BXGC0025020 Methyl (2R)-2-Amino-3-Sulfanylpropanoate 135.04
BXGC0025050 Diethyl 2,6-Dimethyl-4-Phenylpyridine-3,5-Dicarboxylate 327.15
BXGC0025200 2-Anilinonaphthalene-1,4-Dione 249.08
BXGC0025231 Betunolic Acid 454.34
BXGC0025298 6-Methoxyquinoline-4-Carboxylic Acid 203.06
BXGC0025757 Calcimycin 523.27
BXGC0025862 Levothyroxine 776.69
BXGC0026480 Osajin 404.16
BXGC0026528 Cedrol 222.2
BXGC0026607 epiberberine 336.12
BXGC0026935 Triclosan 287.95
BXGC0027259 Tryptanthrin 248.06
BXGC0027374 Glyburide 493.14
BXGC0027421 Paclitaxel 853.33
BXGC0027456 Acetosyringone 196.07
BXGC0027544 Gedunin 482.23
BXGC0027583 dihydroartemisinin 284.16
BXGC0028001 Beta-Lapachone 242.09
BXGC0028278 Rutaecarpine 287.11
BXGC0028562 Methyl Undec-10-Enoate 198.16
BXGC0029234 Gluconolactone 178.05
BXGC0029291 Diphyllin 380.09
BXGC0029355 Pregnenolone 316.24
BXGC0030028 (D)-Serine 105.04
BXGC0030138 Colchicine 399.17
BXGC0030197 Prostaglandin B1 336.23
BXGC0030663 Metformin 129.1
BXGC0030685 Physostigmine 275.16
BXGC0030748 ophiocarpine 355.14
BXGC0031067 6,7-Dimethoxy-3H-2-Benzofuran-1-One 194.06
BXGC0031109 2-Prop-1-En-2-Yl-2,3-Dihydrofuro[3,2-G]Chromen-7-One 228.08
BXGC0031622 Podofilox 414.13
BXGC0033130 Benzoin 212.08
BXGC0033223 (13Ar)-3,10-Dimethoxy-6,8,13,13A-Tetrahydro-5H-Isoquinolino[2,1-B]Isoquinoline-2,9-Diol 327.15
BXGC0033357 4-[[(2R)-3,3-Dimethyloxiran-2-Yl]Methoxy]Furo[3,2-G]Chromen-7-One 286.08
BXGC0033648 Chrysanthemic Acid, Ethyl Ester 196.15
BXGC0033758 5,7-Dimethoxy-8-(3-Methylbut-2-Enoyl)Chromen-2-One 288.1
BXGC0034035 Capsaicin 305.2
BXGC0034077 (2Z,4Z)-5-(1,3-Benzodioxol-5-Yl)-1-Piperidin-1-Ylpenta-2,4-Dien-1-One 285.14
BXGC0034256 Rottlerin 516.18
BXGC0034768 Vincristine 824.4
BXGC0034865 2-(3,4-Dimethoxyphenyl)-3-Hydroxy-5,7-Dimethoxychromen-4-One 358.11
BXGC0034956 (E)-1-(2,4-Dihydroxyphenyl)-3-(4-Methoxyphenyl)Prop-2-En-1-One 270.09
BXGC0034968 Dienestrol 266.13
BXGC0035415 R-Nicotine 162.12
BXGC0035817 4-Methoxy-2-Phenylquinoline 235.1
BXGC0036362 Sodium Lauryl Sulfate 265.15
BXGC0037016 4'-Methoxyflavone 252.08
BXGC0037224 Dichloroacetic Acid 127.94
BXGC0037306 Dubinidine 275.12
BXGC0037599 Tanshinone Iia 294.13
BXGC0037718 Ethacrynic Acid 302.01
BXGC0037880 Euparin 216.08
BXGC0038169 (-)-Lobeline 337.2
BXGC0038197 2-Methoxyphenazine 210.08
BXGC0038233 Nalidixic Acid 232.08
BXGC0038316 Cholesterol 386.35
BXGC0038400 [(9R,10R)-8,8-Dimethyl-9-[(Z)-2-Methylbut-2-Enoyl]Oxy-2-Oxo-9,10-Dihydropyrano[2,3-F]Chromen-10-Yl] (Z)-2-Methylbut-2-Enoate 426.17
BXGC0038408 Isopropyl Palmitate 298.29
BXGC0038719 1,6-Dimethyl-1,2-Dihydronaphtho[1,2-G][1]Benzofuran-10,11-Dione 278.09
BXGC0038963 Dichlorvos 219.95
BXGC0039019 Harmol 198.08
BXGC0039485 Rauwolfia Serpentina 352.18
BXGC0039684 Berberine Chloride 336.12
BXGC0039750 Resveratrol 4'-Methyl Ether 242.09
BXGC0040155 Triptolide 360.16
BXGC0040528 2-Picolinic Acid 123.03
BXGC0040949 Hydroxyprogesterone Caproate 428.29
BXGC0041195 Boldine 327.15
BXGC0041240 Atenolol 266.16
BXGC0041544 Phenprobamate 179.09
BXGC0041560 Thiram 239.99
BXGC0041564 Abietic Acid 302.22
BXGC0041900 Cytochalasin B 479.27
BXGC0041911 (2S)-5-(Diaminomethylideneazaniumyl)-2-(Phenylmethoxycarbonylamino)Pentanoate 308.15
BXGC0042046 Actinodaphnine 311.12
BXGC0042091 Dequalinium 456.33
BXGC0042093 Synandone 452.2
BXGC0042189 (2S,3S,4R,5R)-3,4,5,6-Tetrahydroxyoxane-2-Carboxylic Acid 194.04
BXGC0042281 Permethrin 390.08
BXGC0042298 Cocarboxylase 425.04
BXGC0042414 2-[(E)-2-Phenylethenyl]-2,3-Dihydropyran-6-One 200.08
BXGC0042462 Cysteine 121.02
BXGC0042510 Fluoxetine 309.13
BXGC0042852 Skimmianine 259.08
BXGC0042870 Piceatannol 244.07
BXGC0043126 Nicardipine 479.21
BXGC0044200 Menadione 172.05
BXGC0044245 2,4-Dibromo-6-(2,4-Dibromophenoxy)Phenol 497.71
BXGC0044810 Lamivudine 229.05
BXGC0044857 Sp-600125 220.06
BXGC0045254 Sb-202190 331.11
BXGC0045812 Trifluoperazine 407.16
BXGC0045866 Isopropyl Myristate 270.26
BXGC0046281 Cucurbitacin B 558.32
BXGC0046510 Tpck 351.07
BXGC0046559 Paraxanthine 180.06
BXGC0046964 Deacetylgedunin 440.22
BXGC0047086 4-[(2R)-2-[(1R,3R,5S)-3,5-Dimethyl-2-Oxocyclohexyl]-2-Hydroxyethyl]Piperidine-2,6-Dione 281.16
BXGC0047126 Artemether 298.18
BXGC0047127 Hydron;2,3,9,10-Tetramethoxy-6,8,13,13A-Tetrahydro-5H-Isoquinolino[2,1-B]Isoquinoline;Chloride 355.18
BXGC0047169 Hymecromone 176.05
BXGC0047242 Pyridoxal 167.06
BXGC0047692 Gefitinib 446.15
BXGC0047867 Dalfampridine 94.05
BXGC0048657 Pyridoxamine 168.09
BXGC0048661 Nicardipine Hydrochloride 479.21
BXGC0048801 Sid24823998 254.09
BXGC0049049 Haplamine 257.11
BXGC0049477 Moronic Acid 454.34
BXGC0049516 Kainic Acid 213.1
BXGC0049738 Dexibuprofen 206.13
BXGC0049858 Chalcone 208.09
BXGC0050037 Octisalate 250.16
BXGC0050471 Fluorouracil 130.02
BXGC0050754 Cytisine 190.11
BXGC0050816 Galantamine 287.15
BXGC0050854 Ricinine 164.06
BXGC0051524 Ouabain 584.28
BXGC0051660 Endo-Atropine 289.17
BXGC0051982 Mannitol 182.08
BXGC0052374 Reserpine 608.27
BXGC0053161 [(1R,3S,4S)-4,7,7-Trimethyl-3-Bicyclo[2.2.1]Heptanyl] 2-Thiocyanatoacetate 253.11
BXGC0053334 2,3-Diphenylcycloprop-2-En-1-One 206.07
BXGC0053629 Esatenolol 266.16
BXGC0053641 Nagilactone A 348.16
The  target protein-related  foods
Foods
BXGF Id Food Name Scientific Name Food Group Number of compound? Number of compound in food, higher numbers indicate the food are more associated with the protein