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    <!-- http://www.orpha.net/ORDO/Orphanet_183490 -->

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        <rdfs:label>Genetic photodermatosis</rdfs:label>
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        <rdfs:label>Rare hereditary metabolic disease with peripheral neuropathy</rdfs:label>
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        <rdfs:label>Disorder of porphyrin and haem metabolism</rdfs:label>
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        <rdfs:label>Metabolic disease with skin involvement</rdfs:label>
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        <ns3:IAO_0000115>Acute hepatic porphyrias represent a sub-group of porphyrias (see this term) characterized by the occurrence of neuro-visceral attacks with or without cutaneous manifestations. Acute hepatic porphyrias encompass four diseases: acute intermittent porphyria (the most common), variagate porphyria, hereditary coproporphyria, and hereditary deficit of delta-aminolevulinic acid dehydratase (extremely rare) (see these terms).</ns3:IAO_0000115>
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