Disease table
Disease phenotype | OMIM | Gene symbol (chromosome) protein |
Thyrotoxic periodic paralysis, susceptibility to, 2 (7.13) | 613239 | |
Tibial muscular dystrophy, tardive (5.10, 3.26, 4.2, 1.39, 10.42, 10.8, 3.45, 3.33, 12.89) | 600334 | |
Timothy syndrome (10.131, 10.166) | 601005 | |
Torsion dystonia, early onset (16.1) | 128100 | |
Tubular aggregate myopathy 1 (5.33, 5.39) | 160565 | |
Tubular aggregate myopathy 2 (5.34) | 615883 |