Hepatic porphyria

Hepatic porphyria
Classification and external resources
ICD-10	E 80
ICD-9	277.1
MeSH	D017094

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

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References

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

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External links

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

mt, k, c/g/r/p/y/i, f/h/s/l/o/e, a/u, n, m

k, cgrp/y/i, f/h/s/l/o/e, au, n, m, epon

m (A16/C10), i (k, c/g/r/p/y/i, f/h/s/o/e, a/u, n, m)

cell/phys (coag, heme, immu, gran), csfs

rbmg/mogr/tumr/hist, sysi/epon, btst

drug (B1/2/3+5+6), btst, trns

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Last modified on 15 March 2013, at 20:13