Methylmalonic acidemia with homocystinuria, type cblX

Also known as: combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblX, methylmalonic aciduria and homocysteinemia, cblx type, X-linked recessive, methylmalonic aciduria with homocystinuria, type cblX, intellectual disability, X-linked 3, mental retardation, X-linked 3, methylmalonic acidemia and HOMOCYSTEINEMIA, cblX type, methylmalonic acidemia and homocysteinemia type cblX

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