Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Hypesthesia	[NCBI]

Gene	Link	Information Gain
MS	[NCBI]	5.28348e-05
NGF	[NCBI]	2.05764e-05
ELAVL3	[NCBI]	1.41686e-05
BSCL2	[NCBI]	1.15957e-05
TAC1	[NCBI]	1.15557e-05
MFN2	[NCBI]	1.14048e-05
RAB7A	[NCBI]	1.11376e-05
MPZ	[NCBI]	9.89497e-06
PRKCB	[NCBI]	7.86892e-06
VIP	[NCBI]	6.27261e-06
NPY	[NCBI]	5.42549e-06

OMIM	Link	Information gain
corneal hypesthesia, familial	[NCBI]	0.00107364
indifference to pain, congenital, autosomal dominant	[NCBI]	0.000938013
IH	[NCBI]	0.000750767
HSAN2	[NCBI]	0.000190029
hypertrophic neuropathy and cataract	[NCBI]	0.000145155
insensitivity to pain with hyperplastic myelinopathy	[NCBI]	0.000145155
cyprus facial neuromusculoskeletal syndrome	[NCBI]	0.000145155
adie pupil	[NCBI]	0.000108698
neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive	[NCBI]	0.000108698
charcot-marie-tooth disease, axonal, type 2j	[NCBI]	0.000101342
indifference to pain, congenital, autosomal recessive	[NCBI]	8.67829e-05
CIPA	[NCBI]	8.0832e-05
lymphedema-distichiasis syndrome	[NCBI]	7.92529e-05
HNA	[NCBI]	7.78148e-05
NGFB	[NCBI]	7.18305e-05
tyrosinemia, type i	[NCBI]	4.64948e-05
MPZ	[NCBI]	4.36643e-05
AKR1B1	[NCBI]	3.79048e-05
PWS	[NCBI]	2.45514e-05
VIP	[NCBI]	2.04899e-05
NPY	[NCBI]	1.58525e-05
VEGF	[NCBI]	3.04201e-06
SLE	[NCBI]	1.38534e-06