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MeSH keywords -> Related genes, diseases (OMIM)


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01 Hypothyroidism [NCBI]


Gene


Gene Link Information
Gain
01
TRH [NCBI] 0.000915174
TG [NCBI] 0.000479622
TPO [NCBI] 0.000402548
MIR208A [NCBI] 0.000401057
PRL [NCBI] 0.000306655
SLC5A5 [NCBI] 0.000181078
PAX8 [NCBI] 0.000146574
TSHR [NCBI] 0.000123824
FOXE1 [NCBI] 0.000122133
THRSP [NCBI] 0.000115474
NKX2-1 [NCBI] 0.000109921
DIO2 [NCBI] 0.00010941
TSHB [NCBI] 8.03791e-05
POU1F1 [NCBI] 7.66916e-05
MS [NCBI] 7.55426e-05
SHBG [NCBI] 4.41909e-05
LPL [NCBI] 3.85552e-05
DUOX2 [NCBI] 3.79485e-05
VIP [NCBI] 3.60306e-05
PLN [NCBI] 3.4615e-05
AVP [NCBI] 3.40585e-05
MED12 [NCBI] 3.01553e-05
SLC16A2 [NCBI] 2.79453e-05
UCP3 [NCBI] 2.74976e-05
CETP [NCBI] 2.50362e-05
ACHE [NCBI] 2.24247e-05
SLC26A4 [NCBI] 2.23478e-05
NRGN [NCBI] 1.8409e-05
SLC9A3 [NCBI] 1.64053e-05
TTF2 [NCBI] 1.56021e-05
TH [NCBI] 1.55316e-05
CHAT [NCBI] 1.52007e-05
APOB [NCBI] 1.49966e-05
GNAS [NCBI] 1.47383e-05
UBR1 [NCBI] 1.43415e-05
DUOX1 [NCBI] 1.4088e-05
PAM [NCBI] 1.40544e-05
LRPAP1 [NCBI] 1.30454e-05
TTR [NCBI] 1.26747e-05
CS [NCBI] 1.23214e-05
TOMM70A [NCBI] 1.20902e-05
MB [NCBI] 1.18843e-05
EGF [NCBI] 1.17851e-05
OXCT2 [NCBI] 1.0519e-05
TFAM [NCBI] 9.97557e-06
SULT1B1 [NCBI] 9.71125e-06
TFCP2L1 [NCBI] 9.71125e-06
MBP [NCBI] 9.68194e-06
CXCL10 [NCBI] 9.65749e-06
CST3 [NCBI] 9.46525e-06
FSHR [NCBI] 9.328e-06
PTH [NCBI] 8.88617e-06
IYD [NCBI] 8.81424e-06
RASD2 [NCBI] 8.81424e-06
A1CF [NCBI] 7.79988e-06
SECISBP2 [NCBI] 7.79988e-06
UCP1 [NCBI] 7.66542e-06
PPP3CA [NCBI] 6.92494e-06
RCOR1 [NCBI] 6.92494e-06
TRHR [NCBI] 6.92494e-06
VWF [NCBI] 6.85321e-06
RELN [NCBI] 6.65612e-06
PCP4 [NCBI] 6.52154e-06
CTSE [NCBI] 6.35104e-06
LEP [NCBI] 6.33458e-06
DBH [NCBI] 6.32065e-06
CGA [NCBI] 6.19622e-06
GHR [NCBI] 6.12311e-06
ABI2 [NCBI] 6.05446e-06
PPARGC1B [NCBI] 5.48397e-06
TBCE [NCBI] 5.39003e-06
GNMT [NCBI] 5.21672e-06
LRP2 [NCBI] 5.21672e-06
OMP [NCBI] 4.98666e-06
BSND [NCBI] 4.98666e-06
PTPRJ [NCBI] 4.98666e-06
CYP7A1 [NCBI] 4.8494e-06
CNTN2 [NCBI] 4.72273e-06
HOXA5 [NCBI] 4.66289e-06
RETN [NCBI] 4.50372e-06
ALAD [NCBI] 4.44335e-06
NGF [NCBI] 4.40329e-06
GIP [NCBI] 4.36259e-06
GAST [NCBI] 4.29624e-06
MASP2 [NCBI] 4.16143e-06
CAT [NCBI] 4.11904e-06
ATF6 [NCBI] 4.1189e-06
TTF1 [NCBI] 3.95927e-06
NR1H3 [NCBI] 3.94961e-06
STC1 [NCBI] 3.92174e-06
CSRP3 [NCBI] 3.81421e-06
TNFRSF11B [NCBI] 3.67074e-06
SCG5 [NCBI] 3.64986e-06
CTLA4 [NCBI] 3.61071e-06
OAT [NCBI] 3.58867e-06
MTPN [NCBI] 3.41833e-06
LPA [NCBI] 3.41833e-06
PITX1 [NCBI] 3.41833e-06
NCOA2 [NCBI] 3.39168e-06
INS [NCBI] 3.33535e-06
SREBF2 [NCBI] 3.26497e-06
PITX3 [NCBI] 3.2171e-06
IRF6 [NCBI] 3.2171e-06
HES1 [NCBI] 3.12565e-06
NEFM [NCBI] 3.01865e-06
TF [NCBI] 2.99377e-06
GFAP [NCBI] 2.94048e-06
SLC12A1 [NCBI] 2.93824e-06
NKX2-5 [NCBI] 2.65448e-06
EP300 [NCBI] 2.62262e-06
PON1 [NCBI] 2.58942e-06
RBP4 [NCBI] 2.4732e-06
PRKCE [NCBI] 2.33817e-06
PAX2 [NCBI] 2.31267e-06
IL2RA [NCBI] 2.23892e-06
MYOD1 [NCBI] 2.19189e-06
EGFR [NCBI] 2.18142e-06
BDNF [NCBI] 2.06573e-06
IGFBP1 [NCBI] 1.96904e-06
MOG [NCBI] 1.8898e-06
MGP [NCBI] 1.87501e-06
CASR [NCBI] 1.83048e-06
MAP2 [NCBI] 1.72167e-06
NEFL [NCBI] 1.69005e-06
AQP2 [NCBI] 1.62179e-06
PRKCD [NCBI] 1.60714e-06
HLA-DQB1 [NCBI] 1.48456e-06
GHRL [NCBI] 1.47643e-06
TFRC [NCBI] 1.45072e-06
BMP4 [NCBI] 1.401e-06
CP [NCBI] 1.29675e-06
CFTR [NCBI] 1.23294e-06
BAK1 [NCBI] 1.20688e-06
NEFH [NCBI] 1.16716e-06
IGFBP3 [NCBI] 1.15266e-06
CKAP4 [NCBI] 1.11039e-06
GAPDH [NCBI] 8.37678e-07
CHGA [NCBI] 8.34289e-07
PCNA [NCBI] 8.06739e-07
CRP [NCBI] 7.78746e-07
HLA-DRB1 [NCBI] 7.30214e-07
TNF [NCBI] 7.04156e-07
ALB [NCBI] 6.81088e-07
VEGFA [NCBI] 6.70192e-07
TFPI [NCBI] 6.61933e-07
TP63 [NCBI] 6.02458e-07
UMOD [NCBI] 5.5473e-07
IL4 [NCBI] 5.50148e-07
EPO [NCBI] 5.42835e-07
IGF1 [NCBI] 5.41083e-07
ABCB1 [NCBI] 4.2517e-07
BAX [NCBI] 4.12836e-07
TGFB1 [NCBI] 3.71655e-07
COMT [NCBI] 3.27479e-07
AFP [NCBI] 2.98532e-07
ACP5 [NCBI] 2.79714e-07
GJB2 [NCBI] 2.30377e-07
NPY [NCBI] 2.15356e-07
SLC6A4 [NCBI] 2.10366e-07
LIF [NCBI] 2.07155e-07
CCL2 [NCBI] 1.38993e-07
NOS2 [NCBI] 1.05881e-07
IL1RN [NCBI] 9.5461e-08
ADA [NCBI] 8.22344e-08
APOE [NCBI] 8.14883e-08
G6PD [NCBI] 5.67e-08
NOS3 [NCBI] 3.87037e-08
VDR [NCBI] 1.59663e-08
HFE [NCBI] 9.69431e-09
ACE [NCBI] 3.94083e-09
AR [NCBI] 2.87826e-09
CCK [NCBI] 2.59274e-09
MPO [NCBI] 1.13009e-09




OMIM


OMIM Link Information
gain
01
APS2 [NCBI] 0.00265676
thyroid hormonogenesis, genetic defect in, 4 [NCBI] 0.00222651
hashimoto thyroiditis [NCBI] 0.00210699
TG [NCBI] 0.00179734
CHNG2 [NCBI] 0.00155276
TPO [NCBI] 0.00118761
megalocornea-mental retardation syndrome [NCBI] 0.00109496
PRL [NCBI] 0.000900531
thyroid hormonogenesis, genetic defect in, 2a [NCBI] 0.000823054
CHNG1 [NCBI] 0.000764676
thyrotropin deficiency, isolated [NCBI] 0.00071337
CHNG3 [NCBI] 0.000652698
MCOPS6 [NCBI] 0.000503004
hennekam lymphangiectasia-lymphedema syndrome [NCBI] 0.000480827
SLC5A5 [NCBI] 0.000468052
AHO [NCBI] 0.000454062
TSHB [NCBI] 0.000382492
hypothyroidism, athyroidal, with spiky hair and cleft palate [NCBI] 0.000377087
IGAD1 [NCBI] 0.000320195
myeloproliferative syndrome, transient [NCBI] 0.000263751
aneurysm, intracranial berry, 1 [NCBI] 0.000254795
choreoathetosis, hypothyroidism, and neonatal respiratory distress [NCBI] 0.000245703
young-simpson syndrome [NCBI] 0.000235654
FOXE1 [NCBI] 0.000217525
RA [NCBI] 0.000212868
ectodermal dysplasia, hypohidrotic, with hypothyroidism and ciliary dyskinesia [NCBI] 0.000208582
TSHR [NCBI] 0.000188937
VEGF [NCBI] 0.000178141
thyroid hormonogenesis, genetic defect in, 6 [NCBI] 0.000177653
SHBG [NCBI] 0.000155996
thyroid hormonogenesis, genetic defect in, 1 [NCBI] 0.00015411
PAX8 [NCBI] 0.000142847
thyroid hormonogenesis, genetic defect in, 5 [NCBI] 0.000140823
CTNS [NCBI] 0.000126536
CMH [NCBI] 0.000121549
thyrotropin-releasing hormone deficiency [NCBI] 0.000114444
BWS [NCBI] 0.000113961
TNF [NCBI] 0.00011223
pituitary dwarfism with large sella turcica [NCBI] 0.000104234
JBS [NCBI] 9.75569e-05
NKX2-1 [NCBI] 9.74593e-05
POU1F1 [NCBI] 9.15485e-05
graves disease [NCBI] 8.61061e-05
CF [NCBI] 8.54656e-05
PAM [NCBI] 8.37947e-05
BGLAP [NCBI] 8.20901e-05
LPL [NCBI] 8.18332e-05
chondrocalcinosis due to apatite crystal deposition [NCBI] 8.17879e-05
ectodermal dysplasia, hypohidrotic, with hypothyroidism and agenesis of the corpus callosum [NCBI] 8.17879e-05
VIP [NCBI] 7.68854e-05
EGFR [NCBI] 7.36915e-05
dicarboxylicamino aciduria [NCBI] 7.33318e-05
PDS [NCBI] 7.06802e-05
SLC26A4 [NCBI] 6.84656e-05
DUOX2 [NCBI] 6.7273e-05
AVP [NCBI] 6.61631e-05
IDDM12 [NCBI] 6.37796e-05
thyroglossal duct cyst, familial [NCBI] 6.37796e-05
LIPC [NCBI] 5.81227e-05
DIO3 [NCBI] 5.72112e-05
TOMM70A [NCBI] 5.72112e-05
MIRN208 [NCBI] 5.72112e-05
AITD3 [NCBI] 5.55556e-05
atransferrinemia [NCBI] 5.355e-05
osseous heteroplasia, progressive [NCBI] 5.355e-05
APS1 [NCBI] 5.10125e-05
epiphyseal dysplasia, multiple, with early-onset diabetes mellitus [NCBI] 5.01735e-05
crigler-najjar syndrome, type ii [NCBI] 4.87238e-05
lipomatosis, familial benign cervical [NCBI] 4.87238e-05
myotonia congenita, autosomal recessive [NCBI] 4.87238e-05
17-@beta hydroxysteroid dehydrogenase iii deficiency [NCBI] 4.50425e-05
pituitary dwarfism iii [NCBI] 4.39871e-05
TECTB [NCBI] 4.34619e-05
SRG1 [NCBI] 4.34619e-05
EEC3 [NCBI] 4.29993e-05
EPO [NCBI] 4.21941e-05
hyperlipoproteinemia, type i [NCBI] 4.20713e-05
AHDS [NCBI] 4.20713e-05
pseudohypoparathyroidism, type ib [NCBI] 4.20713e-05
JBS [NCBI] 4.11963e-05
SERPINA6 [NCBI] 3.99966e-05
myotonia congenita, autosomal dominant [NCBI] 3.9584e-05
gilbert syndrome [NCBI] 3.88379e-05
DUOX1 [NCBI] 3.8292e-05
weaver syndrome [NCBI] 3.74479e-05
ALMS [NCBI] 3.55782e-05
MB [NCBI] 3.54753e-05
PVALB [NCBI] 3.49456e-05
SIX6 [NCBI] 3.49456e-05
SLE [NCBI] 3.30011e-05
DIO2 [NCBI] 3.24654e-05
ACHE [NCBI] 3.08003e-05
TBS [NCBI] 3.06484e-05
APOB [NCBI] 3.06232e-05
PXE [NCBI] 2.83755e-05
MYH6 [NCBI] 2.74687e-05
down syndrome [NCBI] 2.63533e-05
MPO [NCBI] 2.63355e-05
GNPAT [NCBI] 2.62544e-05
CHAT [NCBI] 2.60009e-05
UCP1 [NCBI] 2.57958e-05
RTN1 [NCBI] 2.51791e-05
CSF1R [NCBI] 2.51791e-05
AD [NCBI] 2.49534e-05
HAE [NCBI] 2.33265e-05
MAG [NCBI] 2.24526e-05
SLC16A2 [NCBI] 2.18096e-05
ATF6 [NCBI] 2.11304e-05
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiency [NCBI] 2.06612e-05
PON1 [NCBI] 1.97317e-05
APOE [NCBI] 1.94064e-05
GNMT [NCBI] 1.93549e-05
TTR [NCBI] 1.84433e-05
PROP1 [NCBI] 1.83419e-05
GAL [NCBI] 1.80222e-05
AFP [NCBI] 1.70352e-05
GHR [NCBI] 1.67685e-05
OMP [NCBI] 1.66127e-05
CEACAM5 [NCBI] 1.63635e-05
TP73L [NCBI] 1.62299e-05
AR [NCBI] 1.60767e-05
TH [NCBI] 1.50012e-05
CST3 [NCBI] 1.48524e-05
CTLA4 [NCBI] 1.48524e-05
PCNA [NCBI] 1.42651e-05
CCK [NCBI] 1.21492e-05
UCP3 [NCBI] 1.15259e-05
GNRH1 [NCBI] 1.15177e-05
NPY [NCBI] 1.13979e-05
F3 [NCBI] 1.05457e-05
KSS [NCBI] 1.04963e-05
THRB [NCBI] 1.03725e-05
AQP2 [NCBI] 1.01969e-05
G6PD [NCBI] 1.01743e-05
MG [NCBI] 9.71375e-06
MYH7 [NCBI] 9.69476e-06
STAT5A [NCBI] 8.64834e-06
OXT [NCBI] 8.51135e-06
MDD [NCBI] 8.18332e-06
apnea, obstructive sleep [NCBI] 7.89639e-06
GHRH [NCBI] 7.8798e-06
FA [NCBI] 7.49387e-06
cortisol 11-beta-ketoreductase deficiency [NCBI] 7.39463e-06
LCAT [NCBI] 7.31852e-06
ADA [NCBI] 6.28841e-06
IGFALS [NCBI] 6.26076e-06
GIP [NCBI] 5.88956e-06
VDR [NCBI] 5.80788e-06
ACADM [NCBI] 5.47822e-06
PWS [NCBI] 4.80215e-06
MBP [NCBI] 3.54394e-06
MAP2 [NCBI] 3.17183e-06
LEP [NCBI] 2.98601e-06
amyloidosis vi [NCBI] 2.97163e-06
GFAP [NCBI] 2.883e-06
SPP1 [NCBI] 2.81863e-06
NPPA [NCBI] 2.40789e-06
PDCD8 [NCBI] 2.40681e-06
TNFRSF11B [NCBI] 2.39983e-06
CVID [NCBI] 2.34698e-06
SOD2 [NCBI] 2.25278e-06
TF [NCBI] 2.23148e-06
NGFB [NCBI] 1.21876e-06
PTH [NCBI] 6.37302e-07
temporal arteritis [NCBI] 6.02591e-07
BDNF [NCBI] 5.60638e-07
CP [NCBI] 5.11801e-07
CRH [NCBI] 3.90473e-07
TFPI [NCBI] 3.11818e-07
CAT [NCBI] 1.71561e-07
ALB [NCBI] 1.53152e-07
COMT [NCBI] 1.43384e-07
EGF [NCBI] 1.12259e-07
RP [NCBI] 7.9532e-08
CD [NCBI] 5.89457e-08
GAPDH [NCBI] 8.89641e-09




Database Center for Life Science