• Porphyria, Acute Intermittent
  Porphyria, Acute Intermittent

  An autosomal dominant porphyria that is due to a deficiency of HYDROXYMETHYLBILANE SYNTHASE in the LIVER, the third enzyme in the 8-enzyme biosynthetic pathway of HEME. Clinic...<br/>Year introduced: 1993
  MeSH
• Porphyria Cutanea Tarda
  Porphyria Cutanea Tarda

  An autosomal dominant or acquired porphyria due to a deficiency of UROPORPHYRINOGEN DECARBOXYLASE in the LIVER. It is characterized by photosensitivity and cutaneous lesions w...<br/>Year introduced: 1995
  MeSH
• F32G8.2 Transmembrane protein [Caenorhabditis elegans]
  F32G8.2 Transmembrane protein [Caenorhabditis elegans]

  Gene ID:185211
  Gene

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