Hepatic porphyria

Hepatic porphyria
Specialty	Endocrinology

Hepatic porphyrias is a form of porphyria in which the enzyme deficiency occurs in the liver.^[1]

Examples include (in order of synthesis pathway):

See also

Erythropoietic porphyria

References

↑ "OMIM - PORPHYRIA, CONGENITAL ERYTHROPOIETIC". Retrieved 2008-12-04.

External links

Classification	D ICD-10: E80 ICD-9-CM: 277.1 MeSH: D017094

Porphyrias,+Hepatic at the US National Library of Medicine Medical Subject Headings (MeSH)
www.drugs-porphyria.com
www.porphyria-europe.com

Heme metabolism disorders (E80, 277.1, 277.4)

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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