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MeSH keywords -> Related genes, diseases (OMIM)


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01 Choroid Diseases [NCBI]

Gene


 Gene Link Information
Gain		 01
CACD [NCBI] 0.00276628
PBCRA1 [NCBI] 0.000296439
AIC [NCBI] 0.000273523
PRPH2 [NCBI] 4.92992e-05
ARMS2 [NCBI] 2.23612e-05
SERPINF1 [NCBI] 1.56765e-05
RAB38 [NCBI] 1.2828e-05
C2 [NCBI] 1.15809e-05
YAP1 [NCBI] 1.14735e-05
CFB [NCBI] 1.11009e-05
TEAD1 [NCBI] 1.10191e-05
HTRA1 [NCBI] 9.52043e-06
CD36 [NCBI] 8.79786e-06
BEST1 [NCBI] 8.71271e-06
GFAP [NCBI] 8.70766e-06
RCVRN [NCBI] 8.57319e-06
RHO [NCBI] 8.3577e-06
TYRP1 [NCBI] 7.8506e-06
PLG [NCBI] 7.53151e-06
CFH [NCBI] 7.31701e-06
SELPLG [NCBI] 6.93328e-06
ATM [NCBI] 5.67427e-06
MOG [NCBI] 5.21442e-06
CXCL12 [NCBI] 4.80902e-06
SOD1 [NCBI] 4.28486e-06
HFE [NCBI] 4.07844e-06
CD68 [NCBI] 3.90499e-06
VEGFA [NCBI] 2.99236e-06
APOE [NCBI] 2.77962e-06



OMIM


 OMIM Link Information
gain		 01
AIC [NCBI] 0.0016763
VRCP [NCBI] 0.00165256
chorioretinal atrophy, progressive bifocal [NCBI] 0.00165256
chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism [NCBI] 0.0014306
CACD [NCBI] 0.000819746
CORD7 [NCBI] 0.000644945
NNO1 [NCBI] 0.000613493
SCRA [NCBI] 0.000208893
ARMD1 [NCBI] 0.000126235
ornithine aminotransferase deficiency [NCBI] 0.000110259
chorioretinal dysplasia-microcephaly-mental retardation syndrome [NCBI] 9.12041e-05
PPCRA [NCBI] 8.84935e-05
cherubism [NCBI] 8.23447e-05
STGD3 [NCBI] 7.79043e-05
TEAD1 [NCBI] 7.48929e-05
sarcoidosis [NCBI] 7.44271e-05
PITPN [NCBI] 7.15158e-05
bartter syndrome, type 3 [NCBI] 6.29905e-05
ELOVL4 [NCBI] 6.15648e-05
COH1 [NCBI] 5.8177e-05
VMD [NCBI] 5.74392e-05
SLE [NCBI] 4.84565e-05
CD [NCBI] 4.21134e-05
PLG [NCBI] 3.46035e-05
PEDF [NCBI] 3.39459e-05
GFAP [NCBI] 3.13012e-05
SOD1 [NCBI] 2.94908e-05
NF1 [NCBI] 2.66674e-05
VEGF [NCBI] 2.54581e-05
temporal arteritis [NCBI] 2.10286e-05
MUC1 [NCBI] 1.87222e-05
VRNI [NCBI] 5.60622e-06
CF [NCBI] 2.06989e-06



Database Center for Life Science