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MeSH keywords -> Related genes, diseases (OMIM)


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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
acanthosis nigricans with muscle cramps and acral enlargement [NCBI] 0.000128309
pseudoatrophoderma colli [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




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