×
Entrez Id:
7253
Gene Symbol:
TSHR
TSHR
0.510
Biomarker
disease
MGD
×
Entrez Id:
50506
Gene Symbol:
DUOX2
DUOX2
0.500
Biomarker
disease
MGD
×
Entrez Id:
7173
Gene Symbol:
TPO
TPO
0.500
Biomarker
disease
MGD
×
Entrez Id:
7201
Gene Symbol:
TRHR
TRHR
0.200
Biomarker
disease
MGD
×
Entrez Id:
7849
Gene Symbol:
PAX8
PAX8
0.200
Biomarker
disease
MGD
×
Entrez Id:
860
Gene Symbol:
RUNX2
RUNX2
0.200
Biomarker
disease
MGD
×
Entrez Id:
2304
Gene Symbol:
FOXE1
FOXE1
0.200
Biomarker
disease
MGD
×
Entrez Id:
7038
Gene Symbol:
TG
TG
0.200
Biomarker
disease
MGD
×
Entrez Id:
7200
Gene Symbol:
TRH
TRH
0.010
Biomarker
disease
BEFREE
Other causes of cretinism include failure of the thyroid gland to respond to TSH and lack of pituitary TSH (or hypothalamic TRH ).
782770
1976
×
Entrez Id:
3479
Gene Symbol:
IGF1
IGF1
0.200
Biomarker
disease
RGD
The effects of thyroid hormone on insulin-like growth factor (IGF) and IGF-binding protein (IGFBP) expression in the neonatal rat: prolonged high expression of IGFBP-2 in methimazole-induced congenital hypothyroidism.
1718729
1991
×
Entrez Id:
3625
Gene Symbol:
INHBB
INHBB
0.200
Biomarker
disease
RGD
Developmental expression of testis messenger ribonucleic acids in the rat following propylthiouracil-induced neonatal hypothyroidism.
7819453
1994
×
Entrez Id:
632
Gene Symbol:
BGLAP
BGLAP
0.200
Biomarker
disease
RGD
Studies on gene expression in calvaria and serum levels of insulin-like growth factor-I and bone Gla protein in the methimazole-induced congenital hypothyroid rat.
7920889
1993
×
Entrez Id:
348
Gene Symbol:
APOE
APOE
0.020
GeneticVariation
disease
BEFREE
Our data suggest that in iodine-deficient areas, the APOE epsilon4 allele is a genetic risk factor for FIDD .
10889546
2000
×
Entrez Id:
7173
Gene Symbol:
TPO
TPO
0.500
Biomarker
disease
CTD_human
Congenital hypothyroidism with goiter in toy fox terriers.
12564727
2003
×
Entrez Id:
7253
Gene Symbol:
TSHR
TSHR
0.510
Biomarker
disease
CTD_human
The W546X mutation of the thyrotropin receptor gene: potential major contributor to thyroid dysfunction in a Caucasian population.
12629076
2003
×
Entrez Id:
7173
Gene Symbol:
TPO
TPO
0.500
Biomarker
disease
CTD_human
Thyroperoxidase gene mutations in congenital goitrous hypothyroidism with total and partial iodide organification defect.
14751036
2003
×
Entrez Id:
348
Gene Symbol:
APOE
APOE
0.020
Biomarker
disease
BEFREE
Our previous study demonstrated that apolipoprotein E (ApoE ) was a genetic risk factor for FIDD in the local area.
15739386
2005
×
Entrez Id:
7253
Gene Symbol:
TSHR
TSHR
0.510
Biomarker
disease
BEFREE
In conclusion, our association results suggest that TSHR gene is not a susceptibility gene for FIDD in the iodine-deficient areas of China.
15911145
2005
×
Entrez Id:
1734
Gene Symbol:
DIO2
DIO2
0.010
Biomarker
disease
BEFREE
In the previous study, we have proposed that DIO2 may protect against FIDD in the iodine-deficient areas of China.
15911145
2005
×
Entrez Id:
50506
Gene Symbol:
DUOX2
DUOX2
0.500
Biomarker
disease
CTD_human
Persistent mild hypothyroidism associated with novel sequence variants of the DUOX2 gene in two siblings.
16134168
2005
×
Entrez Id:
7173
Gene Symbol:
TPO
TPO
0.500
Biomarker
disease
CTD_human
Total iodide organification defect: clinical and molecular characterization of an Italian family.
16187919
2005
×
Entrez Id:
50506
Gene Symbol:
DUOX2
DUOX2
0.500
Biomarker
disease
CTD_human
Three mutations (p.Q36H, p.G418fsX482, and g.IVS19-2A>C) in the dual oxidase 2 gene responsible for congenital goiter and iodide organification defect.
16322276
2006
×
Entrez Id:
7173
Gene Symbol:
TPO
TPO
0.500
Biomarker
disease
CTD_human
Clinical and genetic characteristics of congenital hypothyroidism due to mutations in the thyroid peroxidase (TPO) gene in Israelis.
17381485
2007
×
Entrez Id:
4741
Gene Symbol:
NEFM
NEFM
0.200
Biomarker
disease
RGD
Congenital hypothyroidism is associated with intermediate filament misregulation, glutamate transporters down-regulation and MAPK activation in developing rat brain.
18845185
2008
×
Entrez Id:
4744
Gene Symbol:
NEFH
NEFH
0.200
Biomarker
disease
RGD
Congenital hypothyroidism is associated with intermediate filament misregulation, glutamate transporters down-regulation and MAPK activation in developing rat brain.
18845185
2008