5.1.d

Disorders of niacin and NAD metabolism

  • Nicotinamide mononucleotide adenylyl transferase 1 deficiency (Leber congenital amaurosis 9)
  • NAD synthetase 1 deficiency (Vertebral, cardiac, renal, and limb defects syndrome type 3)
  • Mitochondrial NAD kinase 2 deficiency (2,4-dienoyl-CoA reductase deficiency with hyperlysinemia)
  • NAD(P)HX dehydratase deficiency (CARKD deficiency)
  • NAD(P)HX epimerase deficiency (Apolipoprotein A-I binding protein deficiency)
  • Nicotinamide nucleotide transhydrogenase deficiency (Glucocorticoid deficiency type 4)

Subnetworks

Immagini SNW 344 x 258 px 1

NOMS

Disorders of neuromodulators and other small molecules

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