Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Acanthosis Nigricans	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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