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Up to: Inborn disorder of porphyrin metabolism · Hereditary photodermatosis · Porphyria
Inherited porphyria
Porphyrias constitute a group of eight hereditary metabolic diseases characterized by intermittent neuro-visceral manifestations, cutaneous lesions or by the combination of both.
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Erythropoietic protoporphyria 15 trials Sub-types →
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CPOX-related hereditary coproporphyria 0 trials · 5 incl. sub-types Sub-types →
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HMBS-related hepatic porphyria 0 trials · 5 incl. sub-types Sub-types →
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Cutaneous porphyria 2 trials
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PPOX-related hepatic porphyria 0 trials · 2 incl. sub-types Sub-types →
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UROD-related inherited porphyria 0 trials · 1 incl. sub-types Sub-types →
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Chester porphyria 0 trials