Homocystinuria without methylmalonic aciduria

Homocystinuria without methylmalonic aciduria

Definition

Homocystinuria without methylmalonic aciduria is an inborn error of vitamin B12 (cobalamin) metabolism characterized by megaloblastic anemia, encephalopathy and, sometimes, developmental delay, and associated with homocystinuria and hyperhomocysteinemia. There are three types of homocystinuria without methylmalonic aciduria; cblE, cblG and cblD-variant 1 (cblDv1).

Also known as functional methionine synthase deficiency, homocystinuria without methylmalonic aciduria, methylcobalamin deficiency — per MONDO

Also identified as