Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Lentigo	[NCBI]

Gene	Link	Information Gain
LOC619539	[NCBI]	0.000438875
CNC	[NCBI]	0.000378131
PRKAR1A	[NCBI]	7.03755e-05
PTEN	[NCBI]	1.85195e-05
PTPN11	[NCBI]	1.58536e-05
PPP3R1	[NCBI]	1.30237e-05
SILV	[NCBI]	1.10073e-05
ALCAM	[NCBI]	1.07742e-05
KITLG	[NCBI]	1.04299e-05
MC1R	[NCBI]	8.96411e-06
PCNA	[NCBI]	8.83209e-06
TYRP1	[NCBI]	8.26009e-06
DCT	[NCBI]	7.51089e-06
BRAF	[NCBI]	5.44136e-06
PRL	[NCBI]	3.26419e-06

OMIM	Link	Information gain
lentiginosis, inherited patterned	[NCBI]	0.00252968
leopard syndrome 1	[NCBI]	0.00218462
CNC2	[NCBI]	0.00200072
CNC1	[NCBI]	0.000932316
noonan-like/multiple giant cell lesion syndrome	[NCBI]	0.000170666
PJS	[NCBI]	0.000127562
lentiginosis, centrofacial neurodysraphic	[NCBI]	0.000127341
arterial dissection with lentiginosis	[NCBI]	0.000127341
lentigines	[NCBI]	0.000127341
BRRS	[NCBI]	0.000113362
NS1	[NCBI]	9.7471e-05
CD	[NCBI]	9.17857e-05
OCA3	[NCBI]	7.64978e-05
NF1	[NCBI]	7.40722e-05
ALCAM	[NCBI]	6.56767e-05
PRKAR1A	[NCBI]	5.74238e-05
DCT	[NCBI]	5.69272e-05
cardiofaciocutaneous syndrome	[NCBI]	5.13785e-05
FDH	[NCBI]	4.98764e-05
TNC	[NCBI]	4.18808e-05
MAS	[NCBI]	3.4199e-05
PCNA	[NCBI]	3.3576e-05
PRL	[NCBI]	9.86858e-06