Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Pain Insensitivity, Congenital [NCBI]


Gene


Gene Link Information
Gain
01
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


OMIM Link Information
gain
01
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




Database Center for Life Science