Solute carrier family 2 (facilitated glucose transporter), member 1
6513
Dystonia 9 – 601042
GLUT1 deficiency syndrome 1, infantile onset, severe – 606777
Stomatin-deficient cryohydrocytosis with neurologic defects – 608885
{Epilepsy, idiopathic generalized, susceptibility to, 12} – 614847
GLUT1 deficiency syndrome 2, childhood onset – 612126