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

References

^ "OMIM - PORPHYRIA, CONGENITAL ERYTHROPOIETIC". http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=263700. Retrieved 2008-12-04.

External links

MeSH Porphyrias,+Hepatic
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 · Variegate porphyria · Erythropoietic protoporphyria

Hereditary hyperbilirubinemia
(bilirubin)

unconjugated: Gilbert's syndrome · Crigler-Najjar syndrome · Lucey-Driscoll syndrome

conjugated: Dubin–Johnson syndrome · Rotor syndrome

M: MET

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)

M: MYL

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

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

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