Disease table
Disease phenotype | OMIM | Gene symbol (chromosome) protein |
Thyrotoxic periodic paralysis, susceptibility to, 2 (7.13) | 613239 | |
Tibial muscular dystrophy, tardive (5.10, 3.24, 4.4, 1.32, 10.44, 10.8, 3.39, 3.28, 12.101) | 600334 | |
Timothy syndrome (10.143, 10.179) | 601005 | |
Torsion dystonia, early onset (17.1) | 128100 | |
Tubular aggregate myopathy 1 (5.41, 5.46) | 160565 | |
Tubular aggregate myopathy 2 (5.42) | 615883 |