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MeSH keywords -> Related genes, diseases (OMIM)


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01 Facial Paralysis [NCBI]


Gene


Gene Link Information
Gain
01
MBS3 [NCBI] 0.00067434
MBS2 [NCBI] 0.000335709
HFM [NCBI] 0.00032066
MROS [NCBI] 0.000252075
MBS1 [NCBI] 0.000252075
WG [NCBI] 0.000120194
MS [NCBI] 0.000104254
MIB1 [NCBI] 2.55884e-05
SOX14 [NCBI] 1.62805e-05
PLXNA1 [NCBI] 1.39774e-05
PPP1R12A [NCBI] 1.35059e-05
SOST [NCBI] 1.21519e-05
PHYH [NCBI] 1.19187e-05
AMPD1 [NCBI] 1.15742e-05
NGFR [NCBI] 9.31688e-06
MBP [NCBI] 5.18764e-06




OMIM


OMIM Link Information
gain
01
MBS [NCBI] 0.014579
HCFP1 [NCBI] 0.00432406
HCFP2 [NCBI] 0.00258184
facial palsy, familial recurrent peripheral [NCBI] 0.00258184
cayler cardiofacial syndrome [NCBI] 0.00248043
johnson neuroectodermal syndrome [NCBI] 0.00128253
bulbar palsy, progressive, with sensorineural deafness [NCBI] 0.000465865
OSCS [NCBI] 0.00029888
HFM [NCBI] 0.00029781
BPP [NCBI] 0.000178142
poland syndrome [NCBI] 0.000169384
amyloidosis v [NCBI] 0.000157517
CMDD [NCBI] 0.000152259
charge syndrome [NCBI] 0.000132394
oculopharyngodistal myopathy [NCBI] 0.000129339
deafness, conductive stapedial, with ear malformation and facial palsy [NCBI] 0.000129339
ophthalmoplegia, progressive, with scrotal tongue and mental deficiency [NCBI] 0.000129339
cranial nerves, recurrent paresis of [NCBI] 0.000129339
NF2 [NCBI] 0.000115273
ophthalmoplegic neuromuscular disorder with abnormal mitochondria [NCBI] 0.000106872
pachygyria with mental retardation and seizures [NCBI] 9.28923e-05
SOX14 [NCBI] 8.42364e-05
hyperostosis corticalis generalisata, benign form of worth, with torus palatinus [NCBI] 7.66903e-05
lenz-majewski hyperostotic dwarfism [NCBI] 7.66903e-05
wildervanck syndrome [NCBI] 7.36018e-05
hyperostosis corticalis generalisata [NCBI] 7.36018e-05
OPTA2 [NCBI] 7.10121e-05
GSN [NCBI] 5.86805e-05
HYPP [NCBI] 5.18422e-05
FSHMD1A [NCBI] 4.64892e-05
OCP [NCBI] 4.36525e-05
SDC2 [NCBI] 4.35421e-05
OPMD [NCBI] 3.45196e-05
SOD2 [NCBI] 3.4423e-05
KSS [NCBI] 3.24666e-05
DGS [NCBI] 2.98032e-05
dystrophia myotonica 1 [NCBI] 2.59404e-05
MBP [NCBI] 2.04944e-05
panencephalitis, subacute sclerosing [NCBI] 1.22245e-05
lymphoma, non-hodgkin, familial [NCBI] 9.31249e-06
SLE [NCBI] 1.39142e-06




Database Center for Life Science