EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
   1.21.1.1 | Congenital Hypothyroidism |
18434651 |
Mutations in the iodotyrosine deiodinase gene and hypothyroidism. |
causal interaction
unassigned |
4
0 |
| 1.21.1.1 | Goiter |
443737 |
[Quantitative aspects of iodine metabolism in one case of congenital iodotyrosine deiodinase defect (author's transl)] |
unassigned |
0 |
| 1.21.1.1 | Goiter |
20298747 |
Genetics and phenomics of hypothyroidism and goiter due to iodotyrosine deiodinase (DEHAL1) gene mutations. |
causal interaction
therapeutic application
unassigned |
3
1
0 |
| 1.21.1.1 | Goiter |
21514561 |
Towards the timely diagnosis of hypothyroidism caused by DEHAL1 gene defects. |
causal interaction
diagnostic usage
therapeutic application
unassigned |
4
2
1
0 |
| 1.21.1.1 | Goiter |
24629858 |
Towards the pre-clinical diagnosis of hypothyroidism caused by iodotyrosine deiodinase (DEHAL1) defects. |
causal interaction
diagnostic usage
unassigned |
3
2
0 |
| 1.21.1.1 | Graves Disease |
17322488 |
Characterisation of DEHAL1 expression in thyroid pathologies. |
causal interaction
diagnostic usage
unassigned |
3
1
0 |
| 1.21.1.1 | Hyperthyroidism |
27732086 |
A Nonradioactive DEHAL Assay for Testing Substrates, Inhibitors, and Monitoring Endogenous Activity. |
ongoing research
unassigned |
4
0 |
| 1.21.1.1 | Hypothyroidism |
443737 |
[Quantitative aspects of iodine metabolism in one case of congenital iodotyrosine deiodinase defect (author's transl)] |
unassigned |
0 |
| 1.21.1.1 | Hypothyroidism |
18434651 |
Mutations in the iodotyrosine deiodinase gene and hypothyroidism. |
causal interaction
unassigned |
4
0 |
| 1.21.1.1 | Hypothyroidism |
18765512 |
Molecular characterization of iodotyrosine dehalogenase deficiency in patients with hypothyroidism. |
unassigned |
0 |
