Autosomal erythropoietic protoporphyria
MONDO:0019263Erythropoietic protoporphyria (EPP) is an inherited disorder of the heme metabolic pathway characterized by accumulation of protoporphyrin in blood, erythrocytes and tissues, and cutaneous manifestations of photosensitivity.
Also known as: EPP
4 clinical trials for this condition and its sub-types, 0 tagged with Autosomal erythropoietic protoporphyria itself.
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Browse by category →Sub-types of Autosomal erythropoietic protoporphyria
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Protoporphyria, erythropoietic, 1 2 trials