Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Nystagmus, Congenital [NCBI]

Gene


 Gene Link Information
Gain		 01
NYS4 [NCBI] 0.000438875
FRMD7 [NCBI] 0.000250126
GPR143 [NCBI] 6.335e-05
PAX6 [NCBI] 2.47577e-05
MBNL3 [NCBI] 1.31553e-05
TULP1 [NCBI] 1.10709e-05
SLC16A2 [NCBI] 1.02129e-05
CACNA1F [NCBI] 1.00015e-05
RPE65 [NCBI] 8.1352e-06
MS [NCBI] 7.68417e-06



OMIM


 OMIM Link Information
gain		 01
NYS4 [NCBI] 0.00115589
CBBM [NCBI] 0.000807657
NYS1 [NCBI] 0.000513473
foveal hypoplasia and presenile cataract syndrome [NCBI] 0.00010353
SOX21 [NCBI] 0.000103218
FRMD7 [NCBI] 0.000103218
AHDS [NCBI] 8.74777e-05
CSNB1A [NCBI] 8.27066e-05
ZIC2 [NCBI] 7.46818e-05
OCA1A [NCBI] 7.31286e-05
DM2 [NCBI] 6.97176e-05
SLC16A2 [NCBI] 6.74106e-05
DCT [NCBI] 6.32586e-05
OA1 [NCBI] 5.69979e-05
PAX6 [NCBI] 5.28443e-05
dystrophia myotonica 1 [NCBI] 4.57216e-05



Database Center for Life Science