MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Addison Disease
[NCBI]
Gene
Gene
Link
Information
Gain
01
AIRE
[NCBI]
7.1175e-05
AAAS
[NCBI]
5.3898e-05
ABCD1
[NCBI]
2.37256e-05
HLA-DQB1
[NCBI]
2.24271e-05
PTPN22
[NCBI]
2.22193e-05
HLA-DRB1
[NCBI]
1.99421e-05
CTLA4
[NCBI]
1.94054e-05
POMC
[NCBI]
1.9331e-05
CYP27B1
[NCBI]
1.89357e-05
TPO
[NCBI]
1.85769e-05
MICA
[NCBI]
1.44627e-05
CSAD
[NCBI]
1.24076e-05
CLEC2D
[NCBI]
1.19738e-05
SH2B3
[NCBI]
1.16282e-05
CLEC16A
[NCBI]
1.16282e-05
HLA-DQA1
[NCBI]
1.13062e-05
INS
[NCBI]
1.12054e-05
SOAT2
[NCBI]
1.03605e-05
CD69
[NCBI]
1.00853e-05
PTPN2
[NCBI]
9.84826e-06
FOXP3
[NCBI]
9.4672e-06
IL21
[NCBI]
8.86509e-06
SUMO4
[NCBI]
8.57886e-06
HSD17B1
[NCBI]
8.33377e-06
ERBB3
[NCBI]
7.15981e-06
AVP
[NCBI]
7.02756e-06
STAR
[NCBI]
6.86593e-06
SLC6A2
[NCBI]
6.56643e-06
FCGR3B
[NCBI]
6.41223e-06
IL2RA
[NCBI]
6.24407e-06
HDC
[NCBI]
6.17867e-06
FCGR3A
[NCBI]
6.1532e-06
CYP21A2
[NCBI]
6.04316e-06
DYSF
[NCBI]
5.91777e-06
FCGR2A
[NCBI]
5.85313e-06
CXCL10
[NCBI]
5.42641e-06
CYP17A1
[NCBI]
5.40203e-06
CIITA
[NCBI]
5.40203e-06
ADM
[NCBI]
5.17615e-06
PTPN11
[NCBI]
4.58025e-06
SLC5A5
[NCBI]
4.56563e-06
WAS
[NCBI]
4.35643e-06
IL2
[NCBI]
4.30602e-06
LEP
[NCBI]
4.24516e-06
CCR5
[NCBI]
4.19807e-06
CCR2
[NCBI]
4.10419e-06
CD86
[NCBI]
3.91199e-06
PTH
[NCBI]
3.56072e-06
CALCA
[NCBI]
2.83346e-06
VDR
[NCBI]
2.83346e-06
TRH
[NCBI]
2.78316e-06
TG
[NCBI]
2.7123e-06
PRL
[NCBI]
1.36823e-06
OMIM
OMIM
Link
Information
gain
01
APS2
[NCBI]
0.00790423
hypoadrenocorticism, familial
[NCBI]
0.00361035
ALD
[NCBI]
0.00150197
APS1
[NCBI]
0.00119912
AHC
[NCBI]
0.00036801
ABCD1
[NCBI]
0.000234249
AIRE
[NCBI]
0.000221098
CRH
[NCBI]
0.000201278
FIH
[NCBI]
0.000110462
CD
[NCBI]
8.36779e-05
POMC
[NCBI]
7.62513e-05
SOAT2
[NCBI]
6.75778e-05
SERPINA6
[NCBI]
6.51787e-05
KSS
[NCBI]
6.5029e-05
GCCD1
[NCBI]
6.22947e-05
corticosterone methyloxidase type ii deficiency
[NCBI]
6.22947e-05
lipoid congenital adrenal hyperplasia
[NCBI]
5.74981e-05
autoimmune disease
[NCBI]
5.64954e-05
CTLA4
[NCBI]
3.81919e-05
RTS
[NCBI]
3.7263e-05
GCCR
[NCBI]
3.65987e-05
CYP17A1
[NCBI]
3.6309e-05
SLE
[NCBI]
3.08456e-05
STAR
[NCBI]
2.78921e-05
HDC
[NCBI]
2.36451e-05
LEP
[NCBI]
2.34203e-05
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency
[NCBI]
1.92697e-05
TPO
[NCBI]
1.56749e-05
AVP
[NCBI]
1.3116e-05
WAS
[NCBI]
1.23989e-05
temporal arteritis
[NCBI]
7.38139e-06
VDR
[NCBI]
7.29416e-06
NPPA
[NCBI]
6.49099e-06
TG
[NCBI]
5.17193e-06
PTH
[NCBI]
3.13926e-06
PRL
[NCBI]
3.33708e-07
MG
[NCBI]
5.16324e-08
Database Center for Life Science