EC Number |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
---|
4.2.1.75 | Abortion, Spontaneous |
9472348 |
Dibromochloropropane: epidemiological findings and current questions. |
causal interaction therapeutic application unassigned |
1 4 0 |
4.2.1.75 | Anemia |
265562 |
Levels of delta-aminolevulinate dehydratase, uroporphyrinogen-I synthase, and protoporphyrin IX in erythrocytes from anemic mutant mice. |
causal interaction unassigned |
4 0 |
4.2.1.75 | Anemia, Hemolytic |
21731282 |
Erythrodontia in congenital erythropoietic porphyria. |
causal interaction unassigned |
3 0 |
4.2.1.75 | Anemia, Hemolytic |
22795135 |
Metabolic correction of congenital erythropoietic porphyria with iPSCs free of reprogramming factors. |
causal interaction unassigned |
3 0 |
4.2.1.75 | Anemia, Hemolytic |
24145442 |
Therapeutic potential of proteasome inhibitors in congenital erythropoietic porphyria. |
causal interaction therapeutic application unassigned |
4 4 0 |
4.2.1.75 | Anemia, Hemolytic |
28334762 |
Missense UROS mutations causing congenital erythropoietic porphyria reduce UROS homeostasis that can be rescued by proteasome inhibition. |
causal interaction therapeutic application unassigned |
3 3 0 |
4.2.1.75 | Carcinogenesis |
9472348 |
Dibromochloropropane: epidemiological findings and current questions. |
causal interaction therapeutic application unassigned |
1 4 0 |
4.2.1.75 | Carcinoma |
2060282 |
Mouse mammary carcinoma porphobilinogenase and hydroxymethylbilane synthetase. |
ongoing research therapeutic application unassigned |
4 2 0 |
4.2.1.75 | Coproporphyria, Hereditary |
8621830 |
Congenital erythropoietic porphyria: clinical, biochemical, and enzymatic profile of a severely affected infant. |
diagnostic usage unassigned |
1 0 |
4.2.1.75 | coproporphyrinogen oxidase deficiency |
8621830 |
Congenital erythropoietic porphyria: clinical, biochemical, and enzymatic profile of a severely affected infant. |
diagnostic usage unassigned |
1 0 |