Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Uveal Diseases [NCBI]

Gene


 Gene Link Information
Gain		 01
OAT [NCBI] 8.44366e-05
MS [NCBI] 5.28348e-05
GATM [NCBI] 1.15599e-05
RLBP1 [NCBI] 1.05382e-05
PITX1 [NCBI] 1.03273e-05
PITX3 [NCBI] 1.01142e-05
RCVRN [NCBI] 9.65552e-06
TIMP3 [NCBI] 9.30968e-06
NF1 [NCBI] 8.85815e-06
GFAP [NCBI] 4.21468e-06



OMIM


 OMIM Link Information
gain		 01
VRCP [NCBI] 0.00200072
ornithine aminotransferase deficiency [NCBI] 0.00124652
MACOM [NCBI] 0.000844965
CHM [NCBI] 0.000723233
glaucoma-related pigment dispersion syndrome [NCBI] 0.000611315
SCRA [NCBI] 0.000205943
deafness, conductive, with stapes fixation [NCBI] 0.000157769
iris pigment layer, cleavage of [NCBI] 0.000133566
macular dystrophy, fenestrated sheen type [NCBI] 0.000133566
fundus dystrophy, pseudoinflammatory, recessive form [NCBI] 0.00010262
choroideremia with deafness and obesity [NCBI] 9.71155e-05
VRNI [NCBI] 9.04444e-05
PPCRA [NCBI] 8.70536e-05
bietti crystalline corneoretinal dystrophy [NCBI] 8.4734e-05
SFD [NCBI] 7.40678e-05
XFS [NCBI] 7.19808e-05
PPCD1 [NCBI] 7.10309e-05
CMTX1 [NCBI] 5.96384e-05
COL18A1 [NCBI] 5.44203e-05
TIMP3 [NCBI] 4.73293e-05
WT1 [NCBI] 4.352e-05
ZS [NCBI] 4.0314e-05
PXE [NCBI] 3.0197e-05
SLE [NCBI] 1.4722e-05
RP [NCBI] 1.44766e-05
GFAP [NCBI] 5.1522e-06
CEACAM5 [NCBI] 1.44627e-06



Database Center for Life Science