Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Lacrimal Apparatus Diseases [NCBI]


Gene


Gene Link Information
Gain
01
CORD8 [NCBI] 0.000438875
AAAS [NCBI] 0.000285379
WG [NCBI] 0.000222409
FOXD2 [NCBI] 1.50142e-05
LACRT [NCBI] 1.35324e-05
JARID1D [NCBI] 1.27529e-05
SOAT2 [NCBI] 1.14848e-05
EGF [NCBI] 9.98549e-06
SALL1 [NCBI] 9.50277e-06
PBX1 [NCBI] 8.69421e-06
CD79A [NCBI] 7.36102e-06
BCL10 [NCBI] 7.2953e-06
TWIST1 [NCBI] 7.01106e-06
CD22 [NCBI] 6.60566e-06
FGFR3 [NCBI] 5.07883e-06
HRAS [NCBI] 3.65685e-06
CD68 [NCBI] 3.32487e-06
GFAP [NCBI] 2.61568e-06
PCNA [NCBI] 2.29333e-06




OMIM


OMIM Link Information
gain
01
alacrima, congenital [NCBI] 0.00123814
palpebral coloboma-lipoma syndrome [NCBI] 0.000938013
CORD8 [NCBI] 0.00088464
AAA [NCBI] 0.000719805
branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and premature aging [NCBI] 0.000672411
AAAS [NCBI] 0.000227483
vestibulocochlear dysfunction, progressive [NCBI] 0.000127588
SOAT2 [NCBI] 8.00936e-05
APS1 [NCBI] 5.87887e-05
PHEX [NCBI] 4.87592e-05
EGF [NCBI] 4.07407e-05
lymphoma, non-hodgkin, familial [NCBI] 2.68562e-05
NF1 [NCBI] 2.66674e-05
MUC1 [NCBI] 1.87222e-05
GFAP [NCBI] 9.20486e-06
PCNA [NCBI] 7.63229e-06




Database Center for Life Science