EC Number |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
---|
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 | Hypothyroidism |
443737 |
[Quantitative aspects of iodine metabolism in one case of congenital iodotyrosine deiodinase defect (author's transl)] |
unassigned |
0 |
1.21.1.1 | Thyroid Diseases |
5913151 |
Iodotyrosine deiodinase isozymes in the normal and in thyroid diseases. |
ongoing research unassigned |
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 | Thyroid Cancer, Papillary |
17322488 |
Characterisation of DEHAL1 expression in thyroid pathologies. |
causal interaction diagnostic usage unassigned |
3 1 0 |
1.21.1.1 | Thyroid Carcinoma, Anaplastic |
17322488 |
Characterisation of DEHAL1 expression in thyroid pathologies. |
causal interaction diagnostic usage unassigned |
3 1 0 |
1.21.1.1 | Thyroid Neoplasms |
17322488 |
Characterisation of DEHAL1 expression in thyroid pathologies. |
causal interaction diagnostic usage unassigned |
3 1 0 |
1.21.1.1 | Thyroid Nodule |
17322488 |
Characterisation of DEHAL1 expression in thyroid pathologies. |
causal interaction diagnostic usage unassigned |
3 1 0 |
1.21.1.1 | Thyrotoxicosis |
17322488 |
Characterisation of DEHAL1 expression in thyroid pathologies. |
causal interaction diagnostic usage unassigned |
3 1 0 |
1.21.1.1 | Congenital Hypothyroidism |
18434651 |
Mutations in the iodotyrosine deiodinase gene and hypothyroidism. |
causal interaction unassigned |
4 0 |