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MeSH keywords -> Related genes, diseases (OMIM)


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01 Laryngeal Diseases [NCBI]


Gene


Gene Link Information
Gain
01
GER [NCBI] 0.00190747
CD68 [NCBI] 1.97133e-05
LAMB3 [NCBI] 1.59751e-05
EYA1 [NCBI] 9.87506e-06
KRT5 [NCBI] 8.72081e-06
KRT14 [NCBI] 8.39593e-06
SPP1 [NCBI] 8.13281e-06
EGFR [NCBI] 8.10845e-06
CREBBP [NCBI] 7.55162e-06
CD44 [NCBI] 7.48364e-06
TP63 [NCBI] 6.59584e-06
MMP9 [NCBI] 6.16588e-06
FASLG [NCBI] 3.80897e-06
PCNA [NCBI] 3.51758e-06
TNF [NCBI] 1.75645e-06




OMIM


OMIM Link Information
gain
01
DIP [NCBI] 0.000900049
hypertelorism with esophageal abnormality and hypospadias [NCBI] 0.00059777
laryngomalacia [NCBI] 0.000277646
alopecia universalis congenita, xy gonadal dysgenesis, and laryngomalacia [NCBI] 0.000138346
laryngeal web, familial [NCBI] 0.000115876
LOCS [NCBI] 0.000101892
epidermolysis bullosa herpetiformis, dowling-meara type [NCBI] 8.74777e-05
PC1 [NCBI] 7.99881e-05
lipoid proteinosis of urbach and wiethe [NCBI] 7.03584e-05
KRT14 [NCBI] 5.90902e-05
KRT5 [NCBI] 5.79854e-05
TNC [NCBI] 4.61971e-05
EGFR [NCBI] 3.78169e-05
HD [NCBI] 2.70459e-05
SLE [NCBI] 2.62883e-05
PCNA [NCBI] 1.38818e-05
RA [NCBI] 1.35154e-05
MG [NCBI] 7.88196e-06
TNF [NCBI] 5.89603e-06




Database Center for Life Science