Hereditary coproporphyria

A form of acute hepatic porphyria characterized by the occurrence of neuro-visceral attacks and, more rarely, by the presence of cutaneous lesions.

Also known as: coproporphyrinogen oxidase deficiency, hereditary coproporphyria, CPRO deficiency, Cpo deficiency, Cpox deficiency, Cpx deficiency, HCP, Harderoporphyria

6 clinical trials for this condition and its sub-types.