EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    4.1.1.37 | Adrenocortical Carcinoma |
2102982 |
Organ porphyrins and uroporphyrinogen decarboxylase activity in a case of non-functioning adrenocortical carcinoma. |
diagnostic usage
ongoing research
unassigned |
3
1
0 |
| 4.1.1.37 | Azotemia |
6997766 |
Porphyrins in chronic renal failure. |
causal interaction
therapeutic application
unassigned |
3
2
0 |
| 4.1.1.37 | Blister |
31110391 |
Porphyria Cutanea Tarda Presenting as Erythema-multiforme Like Lesions. |
unassigned |
0 |
| 4.1.1.37 | Carcinoma |
1526139 |
Uroporphyrinogen decarboxylase from mouse mammary carcinoma and liver of normal and tumor-bearing mouse. |
ongoing research
therapeutic application
unassigned |
4
1
0 |
| 4.1.1.37 | Carcinoma |
2102982 |
Organ porphyrins and uroporphyrinogen decarboxylase activity in a case of non-functioning adrenocortical carcinoma. |
diagnostic usage
ongoing research
unassigned |
3
1
0 |
| 4.1.1.37 | Carcinoma, Renal Cell |
2716925 |
Uroporphyrinogen decarboxylase and porphyrins in the tissue of human clear-cell renal carcinoma and in its maternal renal cortex. |
diagnostic usage
ongoing research
unassigned |
3
4
0 |
| 4.1.1.37 | Coproporphyria, Hereditary |
398301 |
The porphyrias. |
unassigned |
0 |
| 4.1.1.37 | Coproporphyria, Hereditary |
913057 |
Alterations in the activity of enzymes of haem biosynthesis in lead poisoning and acute hepatic prophyria. |
causal interaction
unassigned |
2
0 |
| 4.1.1.37 | Deficiency Diseases |
3513989 |
Porphyria cutanea tarda, or the uroporphyrinogen decarboxylase deficiency diseases. |
causal interaction
unassigned |
4
0 |
| 4.1.1.37 | Dermatitis |
26908385 |
Porphyria cutanea tarda associated with HFE C282Y homozygosity, iron overload, and use of a contraceptive vaginal ring. |
unassigned |
0 |
