Hereditary cryohydrocytosis with reduced stomatin

Also known as: ChC type 2, hereditary cryohydrocytosis type 2, sdCHC, stomatin-deficient cryohydrocytosis, GLUT1 deficiency syndrome with pseudohyperkalemia and hemolysis, SDCHCN, cryohydrocytosis, stomatin-deficient, with intellectual disability, seizures, cataracts, and massive hepatosplenomegaly, cryohydrocytosis, stomatin-deficient, with mental retardation, seizures, cataracts, and massive hepatosplenomegaly

92 clinical trials for this condition and its sub-types.