साँचा:Heme metabolism disorders देवासंHeme 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 protoporphyriaHereditary hyperbilirubinemia(bilirubin)unconjugated: Gilbert's syndrome · Crigler-Najjar syndrome · Lucey-Driscoll syndrome conjugated: Dubin–Johnson syndrome · Rotor syndrome M: MET mt, a/u/y/n/h, r/g/c/p/i, f/s/l/o, m au/y/n/h, rgcp/i, f/s/l/o, m, epon meds(A16, C10),intm(a/u/y/n/h, r/g/c/p/i, f/s/o) M: MYL cell/phys (coag, heme, immu, gran), csfs rbmg/mogr/tumr/hist, sysi/epon, btst drug (B1/2/3+5+6), btst, trns