Difference between revisions of "Template:Heme metabolism disorders"
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imported>Arcadian (cat) |
imported>Canada Hky (adding Harderoporphyria to porphyrias template) |
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| list2 = <div>''early mitochondrial:'' [[Aminolevulinic acid dehydratase deficiency porphyria|ALAD porphyria]]{{·}} [[Acute intermittent porphyria]]</div> | | list2 = <div>''early mitochondrial:'' [[Aminolevulinic acid dehydratase deficiency porphyria|ALAD porphyria]]{{·}} [[Acute intermittent porphyria]]</div> | ||
<div>''cytoplasmic:'' [[Gunther disease|Gunther disease/congenital erythropoietic porphyria]]{{·}} [[Porphyria cutanea tarda]]/[[Hepatoerythropoietic porphyria]]</div> | <div>''cytoplasmic:'' [[Gunther disease|Gunther disease/congenital erythropoietic porphyria]]{{·}} [[Porphyria cutanea tarda]]/[[Hepatoerythropoietic porphyria]]</div> | ||
| − | <div>''late mitochondrial:'' [[Hereditary coproporphyria]]{{·}} [[Variegate porphyria]]{{·}} [[Erythropoietic protoporphyria]]</div> | + | <div>''late mitochondrial:'' [[Hereditary coproporphyria]]{{·}} [[Harderoporphyria]]{{·}} [[Variegate porphyria]]{{·}} [[Erythropoietic protoporphyria]]</div> |
| group3 = [[Hereditary hyperbilirubinemia]]<br />([[bilirubin]]) | | group3 = [[Hereditary hyperbilirubinemia]]<br />([[bilirubin]]) | ||
