Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


Query MeSH keywords list

01 Dysautonomia, Familial [NCBI]

Gene


 Gene Link Information
Gain		 01
IKBKAP [NCBI] 0.000437677
GER [NCBI] 0.000317425
C9orf4 [NCBI] 1.47753e-05
ELP2 [NCBI] 1.47753e-05
ACTL7B [NCBI] 1.47753e-05
ELP3 [NCBI] 1.38769e-05
C9orf5 [NCBI] 1.38769e-05
ELP4 [NCBI] 1.38769e-05
ACTL7A [NCBI] 1.32935e-05
EPB41L4B [NCBI] 1.32935e-05
NGF [NCBI] 1.23934e-05
CTNNAL1 [NCBI] 1.15742e-05
MYO5A [NCBI] 1.02537e-05
SYP [NCBI] 1.00194e-05
POLR2A [NCBI] 9.57218e-06
MCOLN1 [NCBI] 9.04417e-06
S100A12 [NCBI] 8.60894e-06
LIFR [NCBI] 7.99664e-06
AGER [NCBI] 6.99454e-06
TOR1A [NCBI] 6.37738e-06
IKBKE [NCBI] 5.68167e-06
CHUK [NCBI] 5.50872e-06
IKBKB [NCBI] 5.49849e-06
PRNP [NCBI] 5.38033e-06
TTR [NCBI] 4.70971e-06



OMIM


 OMIM Link Information
gain		 01
HSAN3 [NCBI] 0.00479447
indifference to pain, congenital, autosomal dominant [NCBI] 0.00123814
IKBKAP [NCBI] 0.0009042
CIPA [NCBI] 0.000320683
FFI [NCBI] 0.000205785
neuropathy, hereditary sensorimotor, with upper motor neuron, visual pathway and autonomic disturbance [NCBI] 0.000120229
insensitivity to pain with hyperplastic myelinopathy [NCBI] 0.000120229
dysautonomia-like disorder [NCBI] 0.000120229
ACTL7B [NCBI] 9.02832e-05
ACTL7A [NCBI] 9.02832e-05
C9ORF4 [NCBI] 9.02832e-05
paroxysmal extreme pain disorder [NCBI] 7.97084e-05
AAA [NCBI] 5.30648e-05
MEN2B [NCBI] 4.7895e-05
NGFB [NCBI] 4.71178e-05
WFS1 [NCBI] 4.25659e-05
PRNP [NCBI] 2.78197e-05
TTR [NCBI] 1.77179e-05



Database Center for Life Science