Autoimmune Thyroid Disease, Susceptibility To, 3; Aitd3

Table of contents:

Description
Related genes
Clinical Features
Incidence and onset information
Alternative Names
Researches and researchers
Gene Panels
Sources and references

Genes related to Autoimmune Thyroid Disease, Susceptibility To, 3; Aitd3

TG
ZFAT

View recommended genes panels

Clinical Features

Phenotypes and symptoms related to Autoimmune Thyroid Disease, Susceptibility To, 3; Aitd3

Thyroiditis
Hashimoto thyroiditis

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— No data available about the known clinical features onset.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Autoimmune Thyroid Disease, Susceptibility To, 3; Aitd3 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Congenital Hypothyroidism Deletion/Duplication Panel. By Genetic Services Laboratory University of Chicago (United States). SLC16A2, SLC5A5, TG, THRA, THRB, NKX2-1, TPO, TSHB, KDM6A, DUOX2, UBR1, IYD, GLIS3, DUOXA2, FOXE1, IGSF1, KMT2D, PAX8, SLC26A4, POU1F1 , (...) View the complete list with 1 more genes Panel complete gene list SLC16A2, SLC5A5, TG, THRA, THRB, NKX2-1, TPO, TSHB, KDM6A, DUOX2, UBR1, IYD, GLIS3, DUOXA2, FOXE1, IGSF1, KMT2D, PAX8, SLC26A4, POU1F1, PROP1 Specificity 5 % Genes 50 %
Congenital Hypothyroidism Sequencing Panel. By Genetic Services Laboratory University of Chicago (United States). SLC16A2, SLC5A5, TG, THRA, THRB, NKX2-1, TPO, TSHB, KDM6A, DUOX2, UBR1, IYD, GLIS3, DUOXA2, FOXE1, IGSF1, KMT2D, PAX8, SLC26A4, POU1F1 , (...) View the complete list with 1 more genes Panel complete gene list SLC16A2, SLC5A5, TG, THRA, THRB, NKX2-1, TPO, TSHB, KDM6A, DUOX2, UBR1, IYD, GLIS3, DUOXA2, FOXE1, IGSF1, KMT2D, PAX8, SLC26A4, POU1F1, PROP1 Specificity 5 % Genes 50 %
TG mutation analysis. By Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam (Netherlands). TG Specificity 100 % Genes 50 %
TG. Complete sequencing. By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain). TG Specificity 100 % Genes 50 %
Thyroid dyshormonogenesis 3 (sequence analysis of TG gene). By CGC Genetics (Portugal). TG Specificity 100 % Genes 50 %
Congenital Hypothyroidism and Thyroid Hormone Resistance Sequencing Panel with CNV Detection. By PreventionGenetics PreventionGenetics (United States). SLC16A2, SLC5A5, TG, THRA, THRB, NKX2-1, TPO, TRH, TSHB, DUOX2, UBR1, IYD, NKX2-5, GLIS3, SECISBP2, DUOXA2, FOXE1, GNAS, HESX1, IGSF1 , (...) View the complete list with 4 more genes Panel complete gene list SLC16A2, SLC5A5, TG, THRA, THRB, NKX2-1, TPO, TRH, TSHB, DUOX2, UBR1, IYD, NKX2-5, GLIS3, SECISBP2, DUOXA2, FOXE1, GNAS, HESX1, IGSF1, PAX8, SLC26A4, POU1F1, PROP1 Specificity 5 % Genes 50 %
Congenital Hypothyroidism (Thyroid Dyshormonogenesis) via TG Gene Sequencing with CNV Detection. By PreventionGenetics PreventionGenetics (United States). TG Specificity 100 % Genes 50 %
Thyroid dyshormonogenesis 3. By Centogene AG - the Rare Disease Company (Germany). TG Specificity 100 % Genes 50 %

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Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Symptoms Checker

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