|
OMIM |
Link |
Information gain |
01 |
|
TG
|
[NCBI]
|
0.00335629
|
|
|
hashimoto thyroiditis
|
[NCBI]
|
0.00268434
|
|
|
autoimmune thyroid disease, susceptibility to, 1
|
[NCBI]
|
0.0017432
|
|
|
TPO
|
[NCBI]
|
0.00170205
|
|
|
APS2
|
[NCBI]
|
0.00133015
|
|
|
hyperthyroxinemia, familial
|
[NCBI]
|
0.00108068
|
|
|
autoimmune thyroid disease, susceptibility to, 2
|
[NCBI]
|
0.00078076
|
|
|
candidiasis, familial chronic mucocutaneous, autosomal dominant, with thyroid disease
|
[NCBI]
|
0.00078076
|
|
|
candidiasis, familial chronic mucocutaneous, autosomal recessive
|
[NCBI]
|
0.00072749
|
|
|
thyroid hormonogenesis, genetic defect in, 4
|
[NCBI]
|
0.000656414
|
|
|
candidiasis, familial chronic mucocutaneous, autosomal dominant
|
[NCBI]
|
0.000630242
|
|
|
MNG1
|
[NCBI]
|
0.000630242
|
|
|
GRTH
|
[NCBI]
|
0.00041648
|
|
|
THRB
|
[NCBI]
|
0.000403986
|
|
|
CHNG2
|
[NCBI]
|
0.000263604
|
|
|
graves disease
|
[NCBI]
|
0.000177991
|
|
|
NKX2-1
|
[NCBI]
|
0.000172185
|
|
|
choreoathetosis, hypothyroidism, and neonatal respiratory distress
|
[NCBI]
|
0.000165969
|
|
|
CHNG1
|
[NCBI]
|
0.000130298
|
|
|
thyroid hormone plasma membrane transport defect
|
[NCBI]
|
0.000113808
|
|
|
cutis verticis gyrata, thyroid aplasia, and mental retardation
|
[NCBI]
|
0.000113808
|
|
|
THRA
|
[NCBI]
|
0.000113405
|
|
|
TBG
|
[NCBI]
|
0.000106977
|
|
|
CNC1
|
[NCBI]
|
9.96396e-05
|
|
|
PDS
|
[NCBI]
|
8.93006e-05
|
|
|
APS1
|
[NCBI]
|
6.90605e-05
|
|
|
CD
|
[NCBI]
|
6.88608e-05
|
|
|
hyperthyroidism, nonautoimmune
|
[NCBI]
|
6.73569e-05
|
|
|
thyroid hormonogenesis, genetic defect in, 5
|
[NCBI]
|
6.73569e-05
|
|
|
GRTH
|
[NCBI]
|
6.50476e-05
|
|
|
ODG2
|
[NCBI]
|
6.50476e-05
|
|
|
AITD3
|
[NCBI]
|
6.50476e-05
|
|
|
MAS
|
[NCBI]
|
6.43496e-05
|
|
|
VEGF
|
[NCBI]
|
6.29831e-05
|
|
|
CD86
|
[NCBI]
|
5.07895e-05
|
|
|
DIO1
|
[NCBI]
|
5.07895e-05
|
|
|
ZFAT1
|
[NCBI]
|
5.07895e-05
|
|
|
thyroid hormonogenesis, genetic defect in, 2a
|
[NCBI]
|
4.97207e-05
|
|
|
IPEX
|
[NCBI]
|
4.89242e-05
|
|
|
RA
|
[NCBI]
|
4.65802e-05
|
|
|
MG
|
[NCBI]
|
4.64543e-05
|
|
|
TSHR
|
[NCBI]
|
4.31807e-05
|
|
|
LMOD1
|
[NCBI]
|
4.22403e-05
|
|
|
ZNF331
|
[NCBI]
|
4.22403e-05
|
|
|
PTH
|
[NCBI]
|
4.22076e-05
|
|
|
CD80
|
[NCBI]
|
3.77569e-05
|
|
|
CMD1A
|
[NCBI]
|
3.70584e-05
|
|
|
ADHD
|
[NCBI]
|
3.50501e-05
|
|
|
SIX3
|
[NCBI]
|
3.46975e-05
|
|
|
KLK3
|
[NCBI]
|
3.42635e-05
|
|
|
SLE
|
[NCBI]
|
3.33992e-05
|
|
|
ANGPT2
|
[NCBI]
|
3.13941e-05
|
|
|
PAX8
|
[NCBI]
|
2.82438e-05
|
|
|
LPO
|
[NCBI]
|
2.75956e-05
|
|
|
SHBG
|
[NCBI]
|
2.73601e-05
|
|
|
ECM1
|
[NCBI]
|
2.58813e-05
|
|
|
CYP1B1
|
[NCBI]
|
2.53729e-05
|
|
|
SDHD
|
[NCBI]
|
2.35778e-05
|
|
|
SLC3A1
|
[NCBI]
|
2.35778e-05
|
|
|
CD
|
[NCBI]
|
2.21404e-05
|
|
|
SLC26A4
|
[NCBI]
|
1.91418e-05
|
|
|
CP
|
[NCBI]
|
1.8799e-05
|
|
|
FOXP3
|
[NCBI]
|
1.67499e-05
|
|
|
dystrophia myotonica 1
|
[NCBI]
|
1.25021e-05
|
|
|
PON1
|
[NCBI]
|
1.02047e-05
|
|
|
GAL
|
[NCBI]
|
9.34707e-06
|
|
|
MB
|
[NCBI]
|
8.71723e-06
|
|
|
PTEN
|
[NCBI]
|
7.90208e-06
|
|
|
AR
|
[NCBI]
|
7.23326e-06
|
|
|
PCNA
|
[NCBI]
|
6.18685e-06
|
|
|
EGF
|
[NCBI]
|
5.60404e-06
|
|
|
EGFR
|
[NCBI]
|
5.15697e-06
|
|
|
NPY
|
[NCBI]
|
5.0595e-06
|
|
|
PRL
|
[NCBI]
|
3.89016e-06
|
|
|
MPO
|
[NCBI]
|
3.5314e-06
|
|
|
AD
|
[NCBI]
|
2.54089e-06
|
|
|
TF
|
[NCBI]
|
1.29751e-06
|
|
|
FRAP1
|
[NCBI]
|
1.15662e-06
|
|
|
TFPI
|
[NCBI]
|
1.05579e-06
|
|
|
G6PD
|
[NCBI]
|
1.00031e-06
|
|
|
PGR
|
[NCBI]
|
7.19217e-07
|
|
|
TNFSF6
|
[NCBI]
|
5.78298e-07
|
|
|
CEACAM5
|
[NCBI]
|
5.74408e-07
|
|
|
PPARA
|
[NCBI]
|
1.2983e-07
|
|
|
CRH
|
[NCBI]
|
8.70815e-08
|
|
|
MUC1
|
[NCBI]
|
8.23848e-08
|
|