EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    1.3.3.3 | Coproporphyria, Hereditary |
712737 |
Deficiency of hepatic coproporphyrinogen oxidase in hereditary coproporphyria. |
causal interaction
unassigned |
3
0 |
| 1.3.3.3 | Coproporphyria, Hereditary |
843348 |
Decreased lymphocyte coproporphyrinogen III oxidase activity in hereditary coproporphyria. |
unassigned |
0 |
| 1.3.3.3 | Coproporphyria, Hereditary |
866144 |
[Demonstration of hereditary enzyme defect in coproporphyria] |
diagnostic usage
ongoing research
unassigned |
2
3
0 |
| 1.3.3.3 | Coproporphyria, Hereditary |
913057 |
Alterations in the activity of enzymes of haem biosynthesis in lead poisoning and acute hepatic prophyria. |
causal interaction
unassigned |
2
0 |
| 1.3.3.3 | Coproporphyria, Hereditary |
1733615 |
Fecal coproporphyrin isomers in hereditary coproporphyria. |
diagnostic usage
unassigned |
2
0 |
| 1.3.3.3 | Coproporphyria, Hereditary |
1859268 |
Hereditary coproporphyria: an imitator of multiple sclerosis. |
causal interaction
diagnostic usage
unassigned |
3
4
0 |
| 1.3.3.3 | Coproporphyria, Hereditary |
3574346 |
Analysis of porphyrins and enzymes in porphyrin synthesis in Taenia solium cysticercus from man and pig. |
unassigned |
0 |
| 1.3.3.3 | Coproporphyria, Hereditary |
6181213 |
Coexistence of hereditary coproporphyria and epilepsy: coproporphyrinogen oxidase deficiency in liver and kidney. |
ongoing research
unassigned |
2
0 |
| 1.3.3.3 | Coproporphyria, Hereditary |
6886003 |
Harderoporphyria: a variant hereditary coproporphyria. |
causal interaction
unassigned |
4
0 |
| 1.3.3.3 | Coproporphyria, Hereditary |
7592568 |
Molecular abnormalities of coproporphyrinogen oxidase in patients with hereditary coproporphyria. |
causal interaction
diagnostic usage
unassigned |
3
2
0 |
