MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Pseudohypoparathyroidism
[NCBI]
Gene
Gene
Link
Information
Gain
01
PTH
[NCBI]
0.000821133
GNAS
[NCBI]
0.000807263
HPT
[NCBI]
0.000341765
PTH1R
[NCBI]
1.43319e-05
GHRH
[NCBI]
1.23557e-05
GNG4
[NCBI]
1.13121e-05
GNG3
[NCBI]
1.07289e-05
STX16
[NCBI]
1.07289e-05
GNB5
[NCBI]
1.07289e-05
GNB4
[NCBI]
1.07289e-05
GNG11
[NCBI]
1.02954e-05
GNAI3
[NCBI]
9.95e-06
GNB2
[NCBI]
9.95e-06
GNB1
[NCBI]
9.41701e-06
GNA13
[NCBI]
8.83966e-06
TRPV5
[NCBI]
8.54077e-06
NNAT
[NCBI]
8.06523e-06
TRH
[NCBI]
4.68765e-06
GNB3
[NCBI]
4.21924e-06
FGF23
[NCBI]
3.32718e-06
ACP5
[NCBI]
2.07952e-06
PTHLH
[NCBI]
1.53772e-06
AVP
[NCBI]
1.00438e-06
PRL
[NCBI]
2.6774e-07
OMIM
OMIM
Link
Information
gain
01
AHO
[NCBI]
0.00747098
PTH
[NCBI]
0.00318124
pseudohypoparathyroidism, type ii
[NCBI]
0.00243653
pseudohypoparathyroidism, type ib
[NCBI]
0.00201939
GNAS
[NCBI]
0.00178175
amelogenesis imperfecta, hypoplastic type
[NCBI]
0.000898321
brachydactyly-mental retardation syndrome
[NCBI]
0.000844965
IBGC1
[NCBI]
0.000560268
STX16
[NCBI]
0.000208273
BDE
[NCBI]
0.00014868
osseous heteroplasia, progressive
[NCBI]
0.000144342
SLE
[NCBI]
0.00014353
CHNG1
[NCBI]
0.000124022
PTHR1
[NCBI]
0.000119924
albright hereditary osteodystrophy 2
[NCBI]
0.000110667
MAS
[NCBI]
0.000106707
gnas complex locus, antisense transcript
[NCBI]
6.93505e-05
AIH2
[NCBI]
5.99137e-05
thyrotropin deficiency, isolated
[NCBI]
5.50618e-05
NDP
[NCBI]
2.42502e-05
KSS
[NCBI]
1.56245e-05
PRL
[NCBI]
6.12025e-06
AVP
[NCBI]
1.45669e-06
Database Center for Life Science