| dbo:description
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- Krankheit (de)
- human disease (en)
- մարդու հիվանդություն (hy)
- хвороба людини (uk)
- مرض يصيب الإنسان (ar)
- Condition médicale (fr)
- malattia metabolica trasmessa con modalità autosomica dominante (it)
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- Hydroxymethylbilane Synthase (HMBS) Deficiency (en)
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- Hydroxymethylbilane Synthase Deficiency (en)
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| dbp:genereviewsnbk
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| dbp:icd
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- 277.100000 (xsd:double)
- (en)
- E80.2 (en)
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- Swedish porphyria, pyrroloporphyria, intermittent acute porphyria (en)
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- Acute intermittent porphyria (en)
- برفريا متقطعة حادة (ar)
- Akute intermittierende Porphyrie (de)
- Porphyrie aiguë intermittente (fr)
- 急性間欠性ポルフィリン症 (ja)
- Porfiria acuta intermittente (it)
- Porfiria aguda intermitente (pt)
- Akut intermittent porfyri (sv)
- Острая перемежающаяся порфирия (ru)
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