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01 Congenital Hypothyroidism [NCBI]


Gene


Gene Link Information
Gain
01
TG [NCBI] 0.000237393
PAX8 [NCBI] 0.00021174
TPO [NCBI] 0.000178959
DUOX2 [NCBI] 0.000158383
FOXE1 [NCBI] 0.000142114
SLC5A5 [NCBI] 0.000124959
TSHR [NCBI] 0.000111131
NKX2-1 [NCBI] 0.000104741
TSHB [NCBI] 7.17791e-05
DUOXA2 [NCBI] 5.87532e-05
POU1F1 [NCBI] 4.64826e-05
TTF2 [NCBI] 3.35617e-05
DUOX1 [NCBI] 3.11637e-05
NRGN [NCBI] 2.3578e-05
SLC16A2 [NCBI] 1.66309e-05
TTF1 [NCBI] 1.53985e-05
TPST2 [NCBI] 1.46724e-05
DUOXA1 [NCBI] 1.46724e-05
TRH [NCBI] 1.41372e-05
GLIS3 [NCBI] 1.22923e-05
RCOR1 [NCBI] 9.49893e-06
PCP4 [NCBI] 9.09319e-06
SALL1 [NCBI] 6.7901e-06
ATF6 [NCBI] 6.65546e-06
FOXL2 [NCBI] 6.13914e-06
SLC26A4 [NCBI] 5.74465e-06
HES1 [NCBI] 5.62361e-06
SLC4A1 [NCBI] 5.3847e-06
NKX2-5 [NCBI] 5.12319e-06
GHRH [NCBI] 5.07215e-06
TGM1 [NCBI] 4.97458e-06
PRL [NCBI] 4.83782e-06
GNAS [NCBI] 3.8629e-06
ALB [NCBI] 2.7941e-06
CHAT [NCBI] 2.08121e-06
MOG [NCBI] 2.0671e-06
APOE [NCBI] 1.95693e-06
G6PD [NCBI] 1.61835e-06
VDR [NCBI] 1.4371e-06
PTH [NCBI] 1.15648e-06
NOS2 [NCBI] 8.27615e-07
MBP [NCBI] 8.09163e-07
AFP [NCBI] 3.95149e-07
TNF [NCBI] 2.4193e-07




OMIM


OMIM Link Information
gain
01
CHNG2 [NCBI] 0.00242857
TG [NCBI] 0.000974625
thyroid hormonogenesis, genetic defect in, 2a [NCBI] 0.000938936
CHNG3 [NCBI] 0.000938013
thyroid hormonogenesis, genetic defect in, 3 [NCBI] 0.00088464
CHNG1 [NCBI] 0.000749216
microcephaly, hiatus hernia, and nephrotic syndrome [NCBI] 0.000744944
PCA [NCBI] 0.00072749
TPO [NCBI] 0.000682406
choreoathetosis, hypothyroidism, and neonatal respiratory distress [NCBI] 0.000400687
young-simpson syndrome [NCBI] 0.000385117
DUOX2 [NCBI] 0.000375541
TSHB [NCBI] 0.000349824
thyroid hormonogenesis, genetic defect in, 6 [NCBI] 0.000346585
SLC5A5 [NCBI] 0.000327313
FIDD [NCBI] 0.000310135
thyroid hormonogenesis, genetic defect in, 1 [NCBI] 0.000292061
TSHR [NCBI] 0.000291627
PAX8 [NCBI] 0.000265305
NKX2-1 [NCBI] 0.00020153
POU1F1 [NCBI] 0.00019324
hypothyroidism, athyroidal, with spiky hair and cleft palate [NCBI] 0.000176319
PDS [NCBI] 0.000158512
thyrotropin deficiency, isolated [NCBI] 0.000143313
pituitary dwarfism iii [NCBI] 0.000133288
JBS [NCBI] 0.00011952
diabetes mellitus, neonatal, with congenital hypothyroidism [NCBI] 0.000115302
SLE [NCBI] 9.82747e-05
FOXE1 [NCBI] 9.40846e-05
BWS [NCBI] 7.58419e-05
TPST2 [NCBI] 7.18383e-05
GLIS3 [NCBI] 7.18383e-05
TRS [NCBI] 6.45143e-05
lipomatosis, familial benign cervical [NCBI] 5.96493e-05
AHDS [NCBI] 5.2919e-05
DUOX1 [NCBI] 5.28704e-05
CF [NCBI] 4.36868e-05
CSF1R [NCBI] 3.95875e-05
down syndrome [NCBI] 3.67995e-05
SLC16A2 [NCBI] 3.61208e-05
ATF6 [NCBI] 3.54173e-05
NKX2E [NCBI] 3.25073e-05
PROP1 [NCBI] 3.25073e-05
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiency [NCBI] 3.08094e-05
SLC26A4 [NCBI] 2.61356e-05
AHO [NCBI] 2.58201e-05
ALB [NCBI] 5.70662e-06
CHAT [NCBI] 2.34862e-06
PRL [NCBI] 2.31501e-06
PWS [NCBI] 2.29813e-06
AFP [NCBI] 1.72461e-06
PTH [NCBI] 1.3362e-06
VDR [NCBI] 1.28733e-06
APOE [NCBI] 1.03715e-06
G6PD [NCBI] 4.46861e-07
MBP [NCBI] 1.09201e-07




Database Center for Life Science