EC Number |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
---|
3.1.3.7 | 3'(2'),5'-bisphosphate nucleotidase deficiency |
21549340 |
Chondrodysplasia and abnormal joint development associated with mutations in IMPAD1, encoding the Golgi-resident nucleotide phosphatase, gPAPP. |
causal interaction unassigned |
4 0 |
3.1.3.7 | Anemia |
1179794 |
A longitudinal study of red cell enzymes in infants of low birth weight. |
ongoing research unassigned |
1 0 |
3.1.3.7 | Anemia |
32019729 |
Modulation of sulfur assimilation metabolic toxicity overcomes anemia and hemochromatosis in mice. |
causal interaction ongoing research therapeutic application unassigned |
3 1 4 0 |
3.1.3.7 | Anemia, Iron-Deficiency |
29507250 |
Modulation of intestinal sulfur assimilation metabolism regulates iron homeostasis. |
causal interaction unassigned |
1 0 |
3.1.3.7 | Anemia, Iron-Deficiency |
32019729 |
Modulation of sulfur assimilation metabolic toxicity overcomes anemia and hemochromatosis in mice. |
causal interaction ongoing research therapeutic application unassigned |
3 1 4 0 |
3.1.3.7 | Brachydactyly |
22887726 |
IMPAD1 mutations in two Catel-Manzke like patients. |
causal interaction unassigned |
1 0 |
3.1.3.7 | Cleft Palate |
22887726 |
IMPAD1 mutations in two Catel-Manzke like patients. |
causal interaction unassigned |
1 0 |
3.1.3.7 | Dwarfism |
18695242 |
A role for a lithium-inhibited Golgi nucleotidase in skeletal development and sulfation. |
ongoing research unassigned |
1 0 |
3.1.3.7 | Hemochromatosis |
32019729 |
Modulation of sulfur assimilation metabolic toxicity overcomes anemia and hemochromatosis in mice. |
causal interaction ongoing research therapeutic application unassigned |
3 1 4 0 |
3.1.3.7 | Hyaline Membrane Disease |
212953 |
Fetal lung maturation: human amniotic fluid phosphatidate phosphohydrolase activity through normal gestation and its relation to the lecithin/sphingomyelin ratio. |
unassigned |
0 |