Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Paresthesia	[NCBI]

Gene	Link	Information Gain
MS	[NCBI]	0.000898614
PMP22	[NCBI]	1.53527e-05
NTS	[NCBI]	1.23243e-05
PHYH	[NCBI]	1.08696e-05
IFNA1	[NCBI]	9.99314e-06
MYOM2	[NCBI]	9.96077e-06
SCN9A	[NCBI]	9.72174e-06
SLC12A3	[NCBI]	9.1568e-06
PTPRC	[NCBI]	9.00348e-06
GAA	[NCBI]	8.87975e-06
POLG	[NCBI]	8.81287e-06
MPZ	[NCBI]	8.65629e-06
TRPV1	[NCBI]	8.49915e-06
GDNF	[NCBI]	6.85389e-06
PARK2	[NCBI]	5.76648e-06
JAK2	[NCBI]	5.19736e-06
VIP	[NCBI]	5.04933e-06
CD68	[NCBI]	4.39406e-06
NPY	[NCBI]	4.21356e-06
NGF	[NCBI]	3.57604e-06
PTH	[NCBI]	2.69859e-06

OMIM	Link	Information gain
CTS1	[NCBI]	0.000766909
restless legs syndrome, susceptibility to, 1	[NCBI]	0.000685
meralgia paraesthetica, familial	[NCBI]	0.000148254
HSAN1	[NCBI]	8.16093e-05
NTS	[NCBI]	7.79e-05
alkaptonuria	[NCBI]	7.77866e-05
PARK2	[NCBI]	7.56639e-05
CADASIL	[NCBI]	7.33522e-05
hypertrophic neuropathy of dejerine-sottas	[NCBI]	6.92003e-05
HNPP	[NCBI]	6.73194e-05
CMT1B	[NCBI]	6.67384e-05
CMT1A	[NCBI]	6.3636e-05
glycogen storage disease ii	[NCBI]	5.89806e-05
fabry disease	[NCBI]	5.48332e-05
GAA	[NCBI]	5.17597e-05
AKR1B1	[NCBI]	3.66698e-05
CD	[NCBI]	2.76249e-05
GDNF	[NCBI]	2.51233e-05
TTR	[NCBI]	2.39973e-05
VIP	[NCBI]	1.93093e-05
NPY	[NCBI]	1.4714e-05
NGFB	[NCBI]	1.12723e-05
PTH	[NCBI]	7.00447e-06
KLK3	[NCBI]	6.53707e-06