1.21.1.1 Congenital Hypothyroidism http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=18434651&form=6&db=m Mutations in the iodotyrosine deiodinase gene and hypothyroidism. causal interaction,unassigned 4,0 1.21.1.1 Goiter http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=443737&form=6&db=m [Quantitative aspects of iodine metabolism in one case of congenital iodotyrosine deiodinase defect (author's transl)] unassigned - 1.21.1.1 Goiter http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20298747&form=6&db=m 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 http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21514561&form=6&db=m 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 http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=24629858&form=6&db=m 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 http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17322488&form=6&db=m Characterisation of DEHAL1 expression in thyroid pathologies. causal interaction,diagnostic usage,unassigned 3,1,0 1.21.1.1 Hyperthyroidism http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=27732086&form=6&db=m A Nonradioactive DEHAL Assay for Testing Substrates, Inhibitors, and Monitoring Endogenous Activity. ongoing research,unassigned 4,0 1.21.1.1 Hypothyroidism http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=443737&form=6&db=m [Quantitative aspects of iodine metabolism in one case of congenital iodotyrosine deiodinase defect (author's transl)] unassigned - 1.21.1.1 Hypothyroidism http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=18434651&form=6&db=m Mutations in the iodotyrosine deiodinase gene and hypothyroidism. causal interaction,unassigned 4,0 1.21.1.1 Hypothyroidism http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=18765512&form=6&db=m Molecular characterization of iodotyrosine dehalogenase deficiency in patients with hypothyroidism. unassigned - 1.21.1.1 Hypothyroidism http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20298747&form=6&db=m 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 Hypothyroidism http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21514561&form=6&db=m 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 Hypothyroidism http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=24629858&form=6&db=m 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 Hypothyroidism http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33653783&form=6&db=m Genetic Evaluation of Congenital Hypothyroidism with Gland in situ Using Targeted Exome Sequencing. causal interaction,diagnostic usage,unassigned 3,1,0 1.21.1.1 Intellectual Disability http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21514561&form=6&db=m 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 Intellectual Disability http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=24629858&form=6&db=m 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 iodotyrosine deiodinase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20298747&form=6&db=m 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 iodotyrosine deiodinase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21514561&form=6&db=m 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 iodotyrosine deiodinase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=24629858&form=6&db=m 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 Thyroid Cancer, Papillary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17322488&form=6&db=m Characterisation of DEHAL1 expression in thyroid pathologies. causal interaction,diagnostic usage,unassigned 3,1,0 1.21.1.1 Thyroid Carcinoma, Anaplastic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17322488&form=6&db=m Characterisation of DEHAL1 expression in thyroid pathologies. causal interaction,diagnostic usage,unassigned 3,1,0 1.21.1.1 Thyroid Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=5913151&form=6&db=m Iodotyrosine deiodinase isozymes in the normal and in thyroid diseases. ongoing research,unassigned 2,0 1.21.1.1 Thyroid Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17322488&form=6&db=m Characterisation of DEHAL1 expression in thyroid pathologies. causal interaction,diagnostic usage,unassigned 3,1,0 1.21.1.1 Thyroid Nodule http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17322488&form=6&db=m Characterisation of DEHAL1 expression in thyroid pathologies. causal interaction,diagnostic usage,unassigned 3,1,0 1.21.1.1 Thyrotoxicosis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17322488&form=6&db=m Characterisation of DEHAL1 expression in thyroid pathologies. causal interaction,diagnostic usage,unassigned 3,1,0