Hereditary coproporphyria

MONDO:0007369

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

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

Follow this condition — get notified about new trials

Broader categories

Sort by