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deiodinase deficiency
(phenotype)
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Genetic Markers
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IYD
No SNPs found
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Most Correlated Biogroups
Nitroreductase-like
Nitroreductase
FMN binding
REACTOME_AMINE_DERIVED_HORMONES
aromatic amino acid family metabolic process
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OMIM - Congenital disorder
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Monitoring of deiodinase deficiency based on transcriptomic responses in SH-SY5Y cells.
Molecular characterization of iodotyrosine dehalogenase deficiency in patients with hypothyroidism.
Type 3 deiodinase deficiency causes spatial and temporal alterations in brain T3 signaling that are …
Genetics and phenomics of hypothyroidism and goiter due to iodotyrosine deiodinase (DEHAL1) gene mut…
Type 3 deiodinase deficiency results in functional abnormalities at multiple levels of the thyroid a…
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Most Relevant Clinical Trials
Correction of Selenium Deficiency Has Effect on Thyroid Function
Pharmacogenomic Response to Thyrotropin-Releasing Hormone Stimulation in Healthy Volunteers: The Inf…
Research on Association Between Selenium Deficiencies and Change of Thyroid Function
Swedish Iodine in Pregnancy and Development in Children (SWIDDICH) Study
Quality of Life After Surgery and Radioiodine Treatment
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