Disease table



Disease phenotype
OMIM
Gene symbol (chromosome)
protein
Thyrotoxic periodic paralysis, susceptibility to, 2 (7.13)
613239
KCNJ18 (17p11.2)
Kir2.6 (inwardly rectifying potassium channel 2.6)



Tibial muscular dystrophy, tardive (5.10, 3.26, 4.2, 1.39, 10.42, 10.8, 3.45, 3.33, 12.89)
600334
TTN (2q31)
Titin



Timothy syndrome (10.131, 10.166)
601005
CACNA1C (12p13.33)
Calcium channel, voltage-dependent, L type, alpha 1C subunit



Torsion dystonia, early onset (16.1)
128100
TOR1A (9q34)
Torsin A



Tubular aggregate myopathy 1 (5.33, 5.39)
160565
STIM1 (11p15.4)
Stromal interaction molecule 1



Tubular aggregate myopathy 2 (5.34)
615883
ORAI1 (12q24.31)
ORAI calcium release-activated calcium modulator 1