MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Acanthosis Nigricans
[NCBI]
Gene
Gene
Link
Information
Gain
01
FGFR3
[NCBI]
0.00019617
FGFR2
[NCBI]
3.5307e-05
INSR
[NCBI]
2.59246e-05
IRS1
[NCBI]
1.90977e-05
LMNA
[NCBI]
1.41629e-05
AGPAT2
[NCBI]
1.13583e-05
KRT16
[NCBI]
1.02097e-05
ALMS1
[NCBI]
9.70578e-06
BSCL2
[NCBI]
8.95941e-06
SLC2A3
[NCBI]
8.32635e-06
BMP6
[NCBI]
8.21846e-06
S100A7
[NCBI]
8.16697e-06
KRT10
[NCBI]
8.06843e-06
PIK3R1
[NCBI]
8.02122e-06
MC4R
[NCBI]
7.27826e-06
FGF3
[NCBI]
7.10663e-06
ADRB3
[NCBI]
6.64507e-06
IRS2
[NCBI]
6.35107e-06
SLC2A4
[NCBI]
5.54956e-06
ADRB2
[NCBI]
5.51749e-06
SLC2A1
[NCBI]
4.96046e-06
EGF
[NCBI]
4.79104e-06
SHBG
[NCBI]
4.38298e-06
OMIM
OMIM
Link
Information
gain
01
acanthosis nigricans
[NCBI]
0.00740887
diabetes mellitus, insulin-resistant, with acanthosis nigricans
[NCBI]
0.00130138
lelis syndrome
[NCBI]
0.00092257
INSR
[NCBI]
0.00058692
FGFR3
[NCBI]
0.000333165
cutis gyrata syndrome of beare and stevenson
[NCBI]
0.000331925
ALMS
[NCBI]
0.000233916
CGL2
[NCBI]
0.000230251
FGFR2
[NCBI]
0.000157246
pseudoatrophoderma colli
[NCBI]
0.000128309
acanthosis nigricans with muscle cramps and acral enlargement
[NCBI]
0.000128309
ALMS1
[NCBI]
0.000120022
retinitis pigmentosa, deafness, mental retardation, and hypogonadism
[NCBI]
0.000105843
CGL1
[NCBI]
8.45153e-05
pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities
[NCBI]
7.25761e-05
TGFA
[NCBI]
6.45657e-05
crouzon syndrome
[NCBI]
6.40591e-05
acromegaly
[NCBI]
6.10572e-05
BSCL2
[NCBI]
5.12477e-05
costello syndrome
[NCBI]
4.7895e-05
TD1
[NCBI]
4.18254e-05
CYP19A1
[NCBI]
3.76557e-05
MC4R
[NCBI]
3.57509e-05
LMNA
[NCBI]
2.85927e-05
MODY
[NCBI]
2.62548e-05
DFSP
[NCBI]
2.49961e-05
BWS
[NCBI]
2.07057e-05
AT
[NCBI]
2.00381e-05
SHBG
[NCBI]
1.1027e-05
PWS
[NCBI]
1.03214e-05
EGF
[NCBI]
4.30012e-06
CEACAM5
[NCBI]
3.22435e-08
Database Center for Life Science