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MeSH keywords -> Related genes, diseases (OMIM)


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01 Papilledema [NCBI]

Gene


 Gene Link Information
Gain		 01
TEC [NCBI] 0.000239942
DPYSL5 [NCBI] 1.31488e-05
VEGFA [NCBI] 1.28637e-05
NLRP3 [NCBI] 9.89829e-06
ALB [NCBI] 8.20497e-06
MS [NCBI] 7.68417e-06
CAT [NCBI] 6.33115e-06
PTEN [NCBI] 5.98779e-06
IL1RN [NCBI] 5.8837e-06
EGFR [NCBI] 4.29194e-06



OMIM


 OMIM Link Information
gain		 01
gapo syndrome [NCBI] 0.00111789
intracranial hypertension, idiopathic [NCBI] 0.000219496
pseudopapilledema [NCBI] 0.000219496
pseudopapilledema, ocular hypotelorism, blepharophimosis, and hand anomalies [NCBI] 0.000114122
nonarteritic anterior ischemic optic neuropathy, susceptibility to [NCBI] 9.27854e-05
hyperostosis corticalis generalisata, benign form of worth, with torus palatinus [NCBI] 8.39246e-05
wildervanck syndrome [NCBI] 8.0832e-05
CA1 [NCBI] 7.88574e-05
camurati-engelmann disease [NCBI] 6.56189e-05
mucopolysaccharidosis type vi [NCBI] 6.35713e-05
RP [NCBI] 5.48684e-05
BRRS [NCBI] 5.4349e-05
mucopolysaccharidosis type ii [NCBI] 4.50952e-05
ALB [NCBI] 3.25256e-05
temporal arteritis [NCBI] 2.24422e-05
CAT [NCBI] 2.16261e-05
TS [NCBI] 2.05182e-05
panencephalitis, subacute sclerosing [NCBI] 1.82237e-05
CEACAM5 [NCBI] 1.00944e-05
thrombocytopenic purpura, autoimmune [NCBI] 9.48242e-06
VEGF [NCBI] 5.05168e-06
SLE [NCBI] 1.2705e-06



Database Center for Life Science