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MeSH keywords -> Related genes, diseases (OMIM)


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01 Deglutition Disorders [NCBI]


Gene


Gene Link Information
Gain
01
GER [NCBI] 0.00357266
TARPS [NCBI] 0.000237475
BMP2 [NCBI] 3.20438e-05
MS [NCBI] 2.85481e-05
CTSW [NCBI] 1.47993e-05
MID2 [NCBI] 1.31488e-05
SIL1 [NCBI] 1.20249e-05
HHIP [NCBI] 1.14472e-05
MID1 [NCBI] 1.10938e-05
PABPN1 [NCBI] 1.08696e-05
ATXN7 [NCBI] 1.061e-05
CCL26 [NCBI] 9.69793e-06
CTNS [NCBI] 9.66293e-06
HLA-DRB3 [NCBI] 9.49791e-06
CDC25C [NCBI] 8.16702e-06
MUSK [NCBI] 8.02835e-06
ATXN2 [NCBI] 7.95026e-06
TOR1A [NCBI] 7.2934e-06
CP [NCBI] 6.92894e-06
PSEN1 [NCBI] 6.82737e-06
HP [NCBI] 6.258e-06
KRT7 [NCBI] 6.1534e-06
CCL11 [NCBI] 6.00575e-06
CHEK1 [NCBI] 5.68008e-06
HLA-DRB1 [NCBI] 4.38582e-06
PCNA [NCBI] 2.91614e-06




OMIM


OMIM Link Information
gain
01
hypertelorism with esophageal abnormality and hypospadias [NCBI] 0.00565996
OPMD [NCBI] 0.00212214
megaduodenum and/or megacystis [NCBI] 0.000907667
TARPS [NCBI] 0.000714117
adducted thumbs syndrome [NCBI] 0.000632262
indifference to pain, congenital, autosomal dominant [NCBI] 0.000579249
laryngeal abductor paralysis [NCBI] 0.000539935
gastroesophageal reflux [NCBI] 0.000349722
scleroderma, familial progressive [NCBI] 0.000287577
MAFD6 [NCBI] 0.000254299
MG [NCBI] 0.000245958
SPS [NCBI] 0.000181189
RA [NCBI] 0.00017798
klippel-trenaunay-weber syndrome [NCBI] 0.000127275
insensitivity to pain with hyperplastic myelinopathy [NCBI] 0.000112629
esophageal ring, lower [NCBI] 0.000112629
KSS [NCBI] 0.000101367
CHAC [NCBI] 9.98575e-05
FSHMD1A [NCBI] 9.69594e-05
ophthalmoplegic neuromuscular disorder with abnormal mitochondria [NCBI] 9.01715e-05
odontoma-dysphagia syndrome [NCBI] 9.01715e-05
SLE [NCBI] 8.92081e-05
UCHL3 [NCBI] 8.42364e-05
RSTS [NCBI] 8.31402e-05
dysphasia, familial developmental [NCBI] 8.17048e-05
thalamic degeneration, symmetric infantile [NCBI] 8.17048e-05
dystrophia myotonica 1 [NCBI] 8.15717e-05
AMC [NCBI] 7.97251e-05
pierre robin syndrome [NCBI] 7.6212e-05
MID1 [NCBI] 7.32571e-05
cleft larynx, posterior [NCBI] 6.88829e-05
dystonia, familial, with visual failure and striatal lucencies [NCBI] 6.88829e-05
UCHL1 [NCBI] 6.81758e-05
ATXN2 [NCBI] 6.74106e-05
SRS [NCBI] 6.73532e-05
opitz syndrome [NCBI] 6.00702e-05
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive [NCBI] 5.56647e-05
SNDI [NCBI] 5.56647e-05
SPCH1 [NCBI] 4.70099e-05
HNA [NCBI] 4.55988e-05
PSNP1 [NCBI] 4.43055e-05
alzheimer disease 3 [NCBI] 4.25488e-05
EBR1 [NCBI] 4.20052e-05
MSS [NCBI] 4.09727e-05
CP [NCBI] 3.9521e-05
MJD [NCBI] 3.9186e-05
HP [NCBI] 3.6226e-05
SJS1 [NCBI] 3.52282e-05
HSAN3 [NCBI] 3.45619e-05
GIST [NCBI] 3.38093e-05
CTNS [NCBI] 3.27265e-05
HNPP [NCBI] 3.24418e-05
SCA7 [NCBI] 3.18886e-05
SCA2 [NCBI] 2.68985e-05
apnea, obstructive sleep [NCBI] 2.52912e-05
SCA1 [NCBI] 2.33812e-05
SMAX1 [NCBI] 1.79344e-05
PCNA [NCBI] 1.57012e-05
PD [NCBI] 9.93787e-06
AD [NCBI] 7.78472e-06
panencephalitis, subacute sclerosing [NCBI] 1.78152e-06
PWS [NCBI] 1.24469e-06




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