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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

6 clinical trials for this condition and its sub-types, 5 tagged with Hereditary coproporphyria itself.

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↑ Hepatic porphyria (23) ↑ CPOX-related hereditary coproporphyria (5)

Including sub-types (6) Tagged with Hereditary coproporphyria (5)

Trials to join now! 1 Not yet finished but already full! 2 Completed 1 Terminated 1

Rare disease detection: new study measures porphyria prevalence in symptomatic patients

Knowledge-focused Completed

This completed study aimed to find out how many patients with a certain set of symptoms actually have acute hepatic porphyria (AHP), a rare metabolic disorder. Researchers enrolled 150 adults aged 18 to 60 who had severe abdominal pain along with neurological symptoms like limb w…

Sponsor: Association pour la Recherche en Medecine Interne • Aim: Knowledge-focused

Last updated Jun 27, 2026 09:00 UTC

Hereditary coproporphyria

Where it sits in the disease tree

Rare disease detection: new study measures porphyria prevalence in symptomatic patients