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TTN基因(以及对应的蛋白质)的细胞分布位置:
TTN基因的本体(GO)信息:
疾病名称 | 关系值 | NofPmids | NofSnps | 来源 |
Hereditary Myopathy with Early Respiratory Failure | 0.482714419 | 11 | 1 | BeFree_CLINVAR_CTD_human_ORPHANET_UNIPROT |
TIBIAL MUSCULAR DYSTROPHY, TARDIVE | 0.442442977 | 10 | 3 | BeFree_CLINVAR_MGD_ORPHANET_UNIPROT |
Cardiomyopathy, Dilated, 1g | 0.44 | 3 | 21 | CLINVAR_CTD_human_MGD_UNIPROT |
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9 | 0.36 | 2 | 2 | CLINVAR_CTD_human_UNIPROT |
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2J | 0.32 | 0 | 0 | CTD_human_MGD_ORPHANET |
Cardiomyopathy, Dilated | 0.258411897 | 31 | 2 | BeFree_CLINVAR_CTD_human_GAD_LHGDN |
Myopathy, Early-Onset, with Fatal Cardiomyopathy | 0.240271442 | 1 | 0 | BeFree_CTD_human_ORPHANET |
Myopathy, Centronuclear, Autosomal Recessive | 0.24 | 0 | 1 | CLINVAR_ORPHANET |
Distal Muscular Dystrophies | 0.12680591 | 6 | 0 | BeFree_CTD_human_LHGDN |
Myopathy | 0.125438769 | 10 | 0 | BeFree_CTD_human_LHGDN |
Familial dilated cardiomyopathy | 0.120814326 | 4 | 0 | BeFree_CTD_human |
Muscle Weakness | 0.12 | 1 | 0 | CTD_human |
Eichsfeld type congenital muscular dystrophy | 0.12 | 0 | 0 | ORPHANET |
Myocardial Ischemia | 0.080271442 | 2 | 0 | BeFree_RGD |
Hypertrophic Cardiomyopathy | 0.006905599 | 10 | 0 | BeFree_GAD |
Cardiomyopathies | 0.005981653 | 12 | 0 | BeFree_LHGDN |
Heart Diseases | 0.00408156 | 6 | 0 | BeFree_LHGDN |
Myasthenia Gravis | 0.003257302 | 12 | 1 | BeFree |
Congestive heart failure | 0.002442977 | 9 | 0 | BeFree |
Heart failure | 0.001900093 | 7 | 0 | BeFree |
Thymoma | 0.001628651 | 6 | 0 | BeFree |
Muscular Dystrophies, Limb-Girdle | 0.001628651 | 6 | 0 | BeFree |
Muscular Dystrophy | 0.001357209 | 5 | 0 | BeFree |
Arrhythmogenic Right Ventricular Dysplasia | 0.001085767 | 4 | 0 | BeFree |
Down Syndrome | 0.000814326 | 3 | 0 | BeFree |
Tibial Muscular Dystrophy | 0.000814326 | 3 | 0 | BeFree |
Muscular Dystrophy, Duchenne | 0.000542884 | 2 | 0 | BeFree |
Centronuclear myopathy | 0.000542884 | 2 | 0 | BeFree |
Respiratory Failure | 0.000542884 | 2 | 0 | BeFree |
Inflammatory disorder | 0.000542884 | 2 | 0 | BeFree |
Limb-girdle muscular dystrophy type 2A | 0.000542884 | 2 | 0 | BeFree |
Myofibrillar Myopathy | 0.000542884 | 2 | 0 | BeFree |
Rheumatoid Arthritis | 0.000271442 | 1 | 0 | BeFree |
Restrictive cardiomyopathy | 0.000271442 | 1 | 0 | BeFree |
Coronary Arteriosclerosis | 0.000271442 | 1 | 0 | BeFree |
Dermatomyositis | 0.000271442 | 1 | 0 | BeFree |
Diabetes | 0.000271442 | 1 | 0 | BeFree |
Diabetes Mellitus | 0.000271442 | 1 | 0 | BeFree |
Experimental Autoimmune Encephalomyelitis | 0.000271442 | 1 | 0 | BeFree |
Facial Pain | 0.000271442 | 1 | 0 | BeFree |
Atrial Septal Defects | 0.000271442 | 1 | 0 | BeFree |
HIV Infections | 0.000271442 | 1 | 0 | BeFree |
Ischemia | 0.000271442 | 1 | 0 | BeFree |
Spinal Muscular Atrophy | 0.000271442 | 1 | 0 | BeFree |
Neuromuscular Diseases | 0.000271442 | 1 | 0 | BeFree |
Pain | 0.000271442 | 1 | 0 | BeFree |
Septicemia | 0.000271442 | 1 | 0 | BeFree |
Depressive Symptoms | 0.000271442 | 1 | 1 | BeFree |
Atrophic condition of skin | 0.000271442 | 1 | 0 | BeFree |
Toxic multinodular goiter | 0.000271442 | 1 | 0 | BeFree |
Adult type dermatomyositis | 0.000271442 | 1 | 0 | BeFree |
Sepsis | 0.000271442 | 1 | 0 | BeFree |
Ventricular dilatation (disorder) | 0.000271442 | 1 | 0 | BeFree |
Congenital myopathy (disorder) | 0.000271442 | 1 | 0 | BeFree |
Familial restrictive cardiomyopathy (disorder) | 0.000271442 | 1 | 0 | BeFree |
Malignant neoplasm of prostate | 0.000271442 | 1 | 0 | BeFree |
Overlap syndrome | 0.000271442 | 1 | 0 | BeFree |
Prostate carcinoma | 0.000271442 | 1 | 0 | BeFree |
early pregnancy | 0.000271442 | 1 | 0 | BeFree |
Nemaline Myopathy, Autosomal Recessive | 0.000271442 | 1 | 0 | BeFree |
Becker Muscular Dystrophy | 0.000271442 | 1 | 0 | BeFree |
Heart Failure, Diastolic | 0.000271442 | 1 | 0 | BeFree |
Epithelioma | 0.000271442 | 1 | 0 | BeFree |
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