Template:Heme metabolism disorders
Revision as of 14:26, 15 November 2010 by imported>Arcadian (Dubin–Johnson syndrome)
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| Porphyria, hepatic and erythropoietic (porphyrin) | early mitochondrial: ALAD porphyria · Acute intermittent porphyria
cytoplasmic: Gunther disease/congenital erythropoietic porphyria · Porphyria cutanea tarda/Hepatoerythropoietic porphyria late mitochondrial: Hereditary coproporphyria · Variegate porphyria · Erythropoietic protoporphyria |
|---|---|
| Hereditary hyperbilirubinemia (bilirubin) | unconjugated: Gilbert's syndrome · Crigler-Najjar syndrome · Lucey-Driscoll syndrome conjugated: Dubin–Johnson syndrome · Rotor syndrome |
