641
|
|
|
TNF alpha induced protein 6 |
TSG-6, TSG6 |
Arsenic encephalopathy, Arthritis, Cerebral infraction, Cerebral thrombosis, Dermatitis, Dermatologic disorders, Diabetes mellitus, Diabetic maculopathy, Juvenile arthritis, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Still disease |
642
|
|
|
TNF receptor superfamily member 1A |
CD120a, FPF, TBP1, TNF-R, TNF-R-I, TNF-R55, TNFAR, TNFR1, TNFR55, TNFR60, p55, p55-R, p60 |
Amyloidosis, Ankylosing spondylitis, Anorexia, Arthritis, Autoimmune diseases, Autoinflammatory disease, Behcet syndrome, Biliary cirrhosis, Cerebral ischemia, Cholangitis, Congestive heart failure, Conjunctivitis, Cranial nerve paralysis, Crohn disease, Cystic fibrosis, Cystic fibrosis of pancreas, Diabetes mellitus, Erysipelas, Fasciitis, Heart failure, Hepatic amyloidosis, Intermittent hydrarthrosis, Intermittent joint effusion, Intestinal obstruction, Mental depression, Migraine, Multiple sclerosis, Myocardial infarction, Myositis, Pericarditis, Pleuritis, Psoriasis, Pulmonary cystic fibrosis, Schizophrenia, Biliary cholangitis, Ulcerative colitis, Uveitis, VasculitisView all (23 more) |
643
|
|
|
TNF receptor superfamily member 1B |
CD120b, TBPII, TNF-R-II, TNF-R75, TNFBR, TNFR1B, TNFR2, TNFR80, p75, p75TNFR |
Alopecia, Autism, Cerebral ischemia, Diabetes mellitus, Ectropion, Eczema, Exfoliative dermatitis, Gangrene, Hyperkeratosis, Hypoalbuminemia, Hypothyroidism, Immunologic deficiency syndromes, Liver cirrhosis, Liver fibrosis, Lymphoma, Mental depression, Nail dystrophy, Nervous system diseases, Non-alcoholic fatty liver disease, Obesity, Palmoplantar keratoderma, Paranoid schizophrenia, Poikiloderma, Schizophrenia, Sezary syndrome, Skin neoplasmsView all (11 more) |
644
|
|
|
Troponin C1, slow skeletal and cardiac type |
CMD1Z, CMH13, TN-C, TNC, TNNC |
|
645
|
|
|
Troponin I2, fast skeletal type |
AMCD2B, DA2B, DA2B1, FSSV, fsTnI |
Abnormal spinal segmentation, Arthrogryposis multiplex congenita, Congenital clubfoot, Congenital finger flexion contractures, Digitotalar dysmorphism, Distal arthrogryposis, Dwarfism, High palate, Malocclusion, Micrognathism, Microstomia, Myopathy, Neck webbing, Scoliosis, Sheldon-hall syndrome, Talipes, Tarsal coalition, Vertical talusView all (3 more) |
646
|
|
|
Troponin I3, cardiac type |
CMD1FF, CMD2A, CMH7, RCM1, TNNC1, cTnI |
Cardiomyopathy, Congestive heart failure, Coronary syndrome, Dilated cardiomyopathy, Hearing loss, Heart diseases, Hypertrophic cardiomyopathy, Hypertrophic subaortic stenosis, Left ventricular hypertrophy, Lipoatrophy, Lipodystrophy, Myocardial diseases, Myocardial infarction, Myopathy, Obstructive asymmetric septal hypertrophy, Palmoplantar keratoderma, Restrictive cardiomyopathy, Ventricular hypertrophyView all (3 more) |
647
|
|
|
Troponin T1, slow skeletal type |
ANM, NEM5, STNT, TNT, TNTS |
|
648
|
|
|
Troponin T2, cardiac type |
CMD1D, CMH2, CMPD2, LVNC6, RCM3, TnTC, cTnT |
Congenital alveolar dysplasia, Cardiomyopathy, Cardiovascular diseases, Chronic obstructive pulmonary disease, Congestive heart failure, Coronary syndrome, Dilated cardiomyopathy, Glycogen storage disease, Hearing loss, Heart diseases, Heart failure, Hypertrophic cardiomyopathy, Hypertrophic subaortic stenosis, Left ventricular noncompaction, Lipoatrophy, Lipodystrophy, Myocardial diseases, Myocardial infarction, Myocardial ischemia, Myopathy, Obstructive asymmetric septal hypertrophy, Palmoplantar keratoderma, Restrictive cardiomyopathy, Ventricular tachycardia, Wolff-parkinson-white syndromeView all (10 more) |
649
|
|
|
Troponin T3, fast skeletal type |
DA2B2, TNTF, beta-TnTF |
Abnormal spinal segmentation, Arthrogryposis multiplex congenita, Brachydactyly, Breast cancer, Breast carcinoma, Clinodactyly, Talipes equinovalgus, Congenital camptodactyly, Congenital clubfoot, Digitotalar dysmorphism, Distal arthrogryposis, Dwarfism, High palate, Micrognathism, Microstomia, Neck webbing, Scoliosis, Sheldon-hall syndrome, Talipes, Tarsal coalition, Vertical talusView all (6 more) |
650
|
|
|
Tenascin R |
NEDSTO, TN-R |
|