• Glycogen Storage Disease Type IV
  Glycogen Storage Disease Type IV

  An autosomal recessive metabolic disorder due to a deficiency in expression of glycogen branching enzyme 1 (alpha-1,4-glucan-6-alpha-glucosyltransferase), resulting in an accu...<br/>Year introduced: 1991(1989)
  MeSH
• Hyperoxaluria, Primary
  Hyperoxaluria, Primary

  A genetic disorder characterized by excretion of large amounts of OXALATES in urine; NEPHROLITHIASIS; NEPHROCALCINOSIS; early onset of RENAL FAILURE; and often a generalized d...<br/>Year introduced: 1991(1987)
  MeSH

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on