1.3.3.3	Anemia	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=15579372&form=6&db=m	Adherence modifies the regulation of gene expression induced by interleukin-10.	causal interaction,therapeutic application,unassigned	1,1,0	
1.3.3.3	Anemia, Sideroblastic	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3992190&form=6&db=m	Coproporphyrinogen oxidase activity and porphyrin concentrations in peripheral red blood cells in hereditary sideroblastic anaemia.	ongoing research,therapeutic application,unassigned	4,1,0	
1.3.3.3	Brain Diseases	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=29660996&form=6&db=m	A case of hereditary coproporphyria with posterior reversible encephalopathy and novel coproporphyrinogen oxidase gene mutation c.863T>G (p.Leu288Trp).	unassigned	-	
1.3.3.3	Brain Neoplasms	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21824890&form=6&db=m	Enhanced expression of coproporphyrinogen oxidase in malignant brain tumors: CPOX expression and 5-ALA-induced fluorescence.	causal interaction,diagnostic usage,ongoing research,unassigned	3,3,1,0	
1.3.3.3	Brain Neoplasms	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=23674837&form=6&db=m	Retraction of "Enhanced expression of coproporphyrinogen oxidase in malignant brain tumors: CPOX expression and 5-ALA-induced fluorescence". Neuro-Oncology 13(11):1234-1243.	unassigned	-	
1.3.3.3	Carcinoma	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28416355&form=6&db=m	Expression of coproporphyrinogen oxidase is associated with detection of upper gastrointestinal carcinomas by 5-aminolevulinic acid-mediated photodynamic diagnosis.	causal interaction,diagnostic usage,therapeutic application,unassigned	3,3,1,0	
1.3.3.3	Carcinoma, Hepatocellular	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9674964&form=6&db=m	Effect of acute lead treatment on coproporphyrinogen oxidase activity in HepG2 cells.	ongoing research,unassigned	4,0	
1.3.3.3	Cataract	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=23631845&form=6&db=m	Hereditary cataract of the Nakano mouse: Involvement of a hypomorphic mutation in the coproporphyrinogen oxidase gene.	unassigned	-	
1.3.3.3	Coproporphyria, Hereditary	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=63041&form=6&db=m	The primary enzyme defect in hereditary coproporphyria.	causal interaction,ongoing research,unassigned	1,4,0	
1.3.3.3	Coproporphyria, Hereditary	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=398301&form=6&db=m	The porphyrias.	unassigned	-