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:
Heme metabolism disorders
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t
e
Heme
metabolism disorders
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
Harderoporphyria
Variegate porphyria
Erythropoietic protoporphyria
Hereditary hyperbilirubinemia
(
bilirubin
)
unconjugated:
Gilbert's syndrome
Crigler–Najjar syndrome
Lucey–Driscoll syndrome
conjugated:
Dubin–Johnson syndrome
Rotor syndrome
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