Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Ophthalmology [NCBI]

Gene


 Gene Link Information
Gain		 01



OMIM


 OMIM Link Information
gain		 01
oculodentoosseous dysplasia, recessive [NCBI] 0.000957753
horner syndrome, congenital [NCBI] 0.000892923
achoo syndrome [NCBI] 0.000747314
ADFN [NCBI] 0.000723515
VRNI [NCBI] 0.000672551
HFM [NCBI] 0.000369591
ODDD [NCBI] 0.000183047
RP [NCBI] 0.000167731
CSNBAD3 [NCBI] 0.000133063
OPMD [NCBI] 0.000127116
porencephaly, familial [NCBI] 0.000110729
pierson syndrome [NCBI] 0.000103353
MCDC1 [NCBI] 9.19412e-05
PPCD1 [NCBI] 8.7314e-05
RIEG1 [NCBI] 8.04129e-05
FDH [NCBI] 7.68668e-05
melanoma, uveal [NCBI] 6.79002e-05
DM2 [NCBI] 6.54859e-05
WS1 [NCBI] 6.25412e-05
retbindin [NCBI] 6.1782e-05
BPES [NCBI] 6.06817e-05
CES [NCBI] 5.9313e-05
GLULD1 [NCBI] 5.04217e-05
TRPM3 [NCBI] 4.84003e-05
LAMB2 [NCBI] 4.38507e-05
CHS [NCBI] 4.14313e-05
COCH [NCBI] 3.95298e-05
AQP5 [NCBI] 3.65691e-05
CBD [NCBI] 3.46022e-05
RS1 [NCBI] 3.39677e-05
RA [NCBI] 2.82818e-05
temporal arteritis [NCBI] 2.77061e-05
CJD [NCBI] 1.18245e-05



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