|
661
|
|
|
Trophoblast glycoprotein |
5T4, 5T4AG, M6P1, WAIF1 |
|
|
662
|
|
|
Tumor protein D52 |
D52, N8L, PC-1, PrLZ, hD52 |
|
|
663
|
|
|
TPD52 like 1 |
D53, TPD53 |
|
|
664
|
|
|
Tryptophan hydroxylase 1 |
TPRH, TRPH |
|
|
665
|
|
|
Triosephosphate isomerase 1 |
HEL-S-49, TIM, TPI, TPID |
Alzheimer disease, Anemia, Benign fasciculation-cramp syndrome, Carcinoma, Cholecystitis, Cholelithiasis, Congestive heart failure, Developmental delay, Enzymopathy, Esophagus neoplasm, Hemolytic anemia, Hypertrophic cardiomyopathy, Inborn errors of metabolism, Lung adenocarcinoma, Microangiopathic hemolytic anemia, Mouth neoplasms, Malignant neoplasm of mouth, Myopathy, Nervous system diseases, Neuromuscular diseases, Oppenheim`s disease, Osteoporosis, Peripheral neuropathy, Periventricular leukomalacia, Schizophrenia, Senile dementia, Triosephosphate isomerase deficiencyView all (12 more) |
|
666
|
|
|
Tropomyosin 1 |
C15orf13, CMD1Y, CMH3, HEL-S-265, HTM-alpha, LVNC9, TMSA |
Atrial septal defect, Cardiomyopathy, Congestive heart failure, Dilated cardiomyopathy, Esophagus neoplasm, Hearing loss, Hypertension, Hypertrophic cardiomyopathy, Hypertrophic subaortic stenosis, Left ventricular noncompaction, Lipoatrophy, Lipodystrophy, Myopathy, Obstructive asymmetric septal hypertrophy, Palmoplantar keratoderma, Parkinson disease, Pulmonary atresia with intact ventricular septum, Tetralogy of fallot, Ventricular tachycardiaView all (4 more) |
|
667
|
|
|
Tropomyosin 2 |
AMCD1, CMYO23, CMYP23, DA1, DA2B, DA2B4, HEL-S-273, NEM4, TMSB |
Abnormal spinal segmentation, Acquired kyphoscoliosis, Amyotrophy, Arthrogryposis multiplex congenita, Bulbar palsy, Cap myopathy, Cardiomyopathy, Centronuclear myopathy, Centronuclear myopathy, x-linked, Congenital camptodactyly, Congenital clubfoot, Developmental dysplasia of the hip, Congenital myopathy with fiber type disproportion, Pulmonary hypoplasia, Congenital kyphoscoliosis, Congenital myopathy, Congenital pectus excavatum, Congenital structural myopathy, Cryptorchidism, Digitotalar dysmorphism, Distal arthrogryposis, Dwarfism, Dysphagia, Elbow flexion contracture, Esophagus neoplasm, Facial paralysis, High palate, Hip contracture, Limb muscle atrophy, Mental retardation, Micrognathism, Microstomia, Mitral valve prolapse, Motor delay, Multiple pterygium syndrome, Myopathy, Neck webbing, Nemaline myopathy, Hypotonia, Neuromuscular dysphagia, Pena shokeir syndrome, Ptosis, Scoliosis, Sheldon-hall syndrome, Sinus tachycardia, Talipes, Tarsal coalition, Trismus, Tubular aggregate myopathy, Vertical talusView all (35 more) |
|
668
|
|
|
Tropomyosin 3 |
CAPM1, CFTD, CMYO4A, CMYO4B, CMYP4A, CMYP4B, HEL-189, HEL-S-82p, NEM1, OK/SW-cl.5, TM-5, TM3, TM30, TM30nm, TM5, TPM3nu, TPMsk3, TRK, hscp30 |
Acquired kyphoscoliosis, Adenocarcinoma, Amyotrophy, Anaplastic carcinoma, Arthrogryposis multiplex congenita, Bulbar palsy, Cap myopathy, Carcinoma, Cardiomyopathy, Centronuclear myopathy, Centronuclear myopathy, x-linked, Colonic neoplasms, Congenital clubfoot, Developmental dysplasia of the hip, Congenital myopathy with fiber type disproportion, Congenital hypercontractile muscle stiffness syndrome, Pulmonary hypoplasia, Congenital kyphoscoliosis, Congenital myopathy, Congenital pectus excavatum, Congenital structural myopathy, Cryptorchidism, Distal lower limb amyotrophy, Dwarfism, Dysphagia, Elbow flexion contracture, Facial paralysis, Gastric cancer, High palate, Hip contracture, Inflammatory myofibroblastic tumor, Limb muscle atrophy, Mental retardation, Micrognathism, Mitral valve prolapse, Motor delay, Myopathy, Nemaline myopathy, Hypotonia, Neuromuscular dysphagia, Pena shokeir syndrome, Ptosis, Respiratory failure, Scoliosis, Sinus tachycardia, Stomach neoplasms, Thyroid neoplasm, Thyroid carcinoma, Thyroid gland follicular adenoma, Tubular aggregate myopathyView all (35 more) |
|
669
|
|
|
Tropomyosin 4 |
BDPLT25, HEL-S-108 |
|
|
670
|
|
|
Thiopurine S-methyltransferase |
TPMTD |
|
