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for
congenital hypothyroidism
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
PAX8
IRS4
TSHB
TSHR
THRA
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
endocrine system development
GSE29949_CD8_NEG_DC_SPLEEN_VS_DC_BRAIN_UP
FOXD3_01
HALLMARK_KRAS_SIGNALING_DN
FOXO4_01
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Curated Studies
Most Correlated Studies
Thyroid gene expression profiles of ectopic versus orthotopic tissue
OMIM - Bamforth-Lazarus syndrome
Cancer Gene Census - mutations in cancer genes
OMIM - Disorder of thyroid gland
Mouse Phenotypes - Hypothyroidism
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Literature
Most Relevant Literature
Epidemiology of congenital hypothyroidism: what can be deduced from the Italian registry of infants …
Ultrasound for primary imaging of congenital hypothyroidism.
Experience in treating congenital hypothyroidism: implications regarding free thyroxine and thyrotro…
The Italian screening program for primary congenital hypothyroidism: actions to improve screening, d…
Comparison between liquid and tablet formulations of levothyroxine in the initial treatment of conge…
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Clinical Trials
Most Relevant Clinical Trials
TG Gene Mutations and Congenital Hypothyroidism
Influence of Initial Levothyroxine Dose on Neurodevelopmental and Growth Outcomes in Congenital Hypo…
Clinical and Genetic Analysis in Congenital Hypothyroidism Due to Thyroid Dysgenesis.
The Prevalence of Hearing Loss Among Children With Congenital Hypothyroidism
Targeted Levothyroxine Dosing in Infants With Congenital Hypothyroidism
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