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hereditary coproporphyria | RareConnect | RareConnect.io

/hepatic porphyria

/CPOX-related hereditary coproporphyria

/hereditary coproporphyria

hereditary coproporphyria

Rare Disease

MONDO:0007369

Also Known As

coproporphyrinogen oxidase deficiencyhereditary coproporphyriahereditary coproporphyria porphyriaCPRO deficiencyCpo deficiencyCpox deficiencyCpx deficiencyHCPHarderoporphyriacoproporphyriacoproporphyria hereditarycoproporphyria, hereditaryporphyria hepatica IIporphyria hepatica coproporphyria

Definition

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

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:121300 ↗

Orphanet

Orphanet:79273 ↗

GARD

Related Diseases

erythropoietic protoporphyria

MONDO:0001676

porphyria due to ALA dehydratase deficiency

MONDO:0013000

porphyria cutanea tarda

MONDO:0015104

harderoporphyria

MONDO:0030048

HMBS-related hepatic porphyria

MONDO:0700382

PPOX-related hepatic porphyria

MONDO:0700383

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