Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Pain Insensitivity, Congenital	[NCBI]

Gene	Link	Information Gain
SCN9A	[NCBI]	0.000124586
NTRK1	[NCBI]	9.09357e-05
NGF	[NCBI]	4.87347e-05
KCNIP3	[NCBI]	1.1507e-05
PSEN2	[NCBI]	6.07977e-06

OMIM	Link	Information gain
indifference to pain, congenital, autosomal dominant	[NCBI]	0.00390348
CIPA	[NCBI]	0.00153861
indifference to pain, congenital, autosomal recessive	[NCBI]	0.000906085
NTRK1	[NCBI]	0.000500192
HSAN5	[NCBI]	0.00032567
HSAN2	[NCBI]	0.000261675
NGFB	[NCBI]	0.000200332
corneal hypesthesia with retinal abnormalities, sensorineural deafness, unusual facies, persistent ductus arteriosus, and mental retardation	[NCBI]	0.000130439
insensitivity to pain with hyperplastic myelinopathy	[NCBI]	0.000130439
SCN9A	[NCBI]	0.000129851
cerebellotrigeminal dermal dysplasia	[NCBI]	8.66409e-05