Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Exophthalmos [NCBI]


Gene


Gene Link Information
Gain
01
PRL [NCBI] 1.86595e-05
CD68 [NCBI] 1.30251e-05
XCL1 [NCBI] 1.14023e-05
CD52 [NCBI] 8.82969e-06
PAX3 [NCBI] 8.30369e-06
FOXO1 [NCBI] 8.24625e-06
CD99 [NCBI] 7.87919e-06
TRH [NCBI] 5.78787e-06
ACHE [NCBI] 5.40614e-06
AFP [NCBI] 4.36229e-06




OMIM


OMIM Link Information
gain
01
CMDR [NCBI] 0.000840405
robinow syndrome, autosomal dominant [NCBI] 0.000676229
NLS [NCBI] 0.000626005
RNS [NCBI] 0.000438008
bone fragility with craniosynostosis, ocular proptosis, hydrocephalus, and distinctive facial features [NCBI] 0.000109365
microcephaly, corpus callosum dysgenesis, and cleft lip/palate [NCBI] 0.000109365
acrofrontofacionasal dysostosis, severe [NCBI] 0.000109365
PRL [NCBI] 9.65776e-05
desmosterolosis [NCBI] 9.65043e-05
GRTH [NCBI] 9.14716e-05
ABS [NCBI] 6.93203e-05
graves disease [NCBI] 6.72698e-05
RBS [NCBI] 6.54521e-05
CRMO [NCBI] 5.67342e-05
MG [NCBI] 3.7561e-05
ACHE [NCBI] 2.48822e-05
AFP [NCBI] 1.9185e-05
RA [NCBI] 1.1009e-05
SLE [NCBI] 4.85239e-06




Database Center for Life Science