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MeSH keywords -> Related genes, diseases (OMIM)


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01 Iris Diseases [NCBI]


Gene


Gene Link Information
Gain
01
CHED1 [NCBI] 0.000415947
PITX2 [NCBI] 2.4684e-05
GPR143 [NCBI] 2.42373e-05
TYRP1 [NCBI] 2.01213e-05
PAX6 [NCBI] 1.74197e-05
RAB38 [NCBI] 1.378e-05
C1QTNF5 [NCBI] 1.33737e-05
COL8A2 [NCBI] 1.277e-05
SLC4A11 [NCBI] 1.25327e-05
PITX1 [NCBI] 1.01952e-05
PITX3 [NCBI] 9.98211e-06
ZBTB16 [NCBI] 9.68406e-06
TYR [NCBI] 9.04228e-06
MITF [NCBI] 8.11597e-06
NKX2-1 [NCBI] 7.13349e-06
KRT7 [NCBI] 7.02375e-06
VEGFA [NCBI] 3.89405e-06




OMIM


OMIM Link Information
gain
01
iris pigment epithelium anomalies [NCBI] 0.0032967
glaucoma-related pigment dispersion syndrome [NCBI] 0.00123297
ataxia, spastic, with congenital miosis [NCBI] 0.00108068
ectopia lentis with ectopia of pupil [NCBI] 0.00072749
aniridia, cerebellar ataxia, and mental deficiency [NCBI] 0.000588308
branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and premature aging [NCBI] 0.00051629
IRID2 [NCBI] 0.000326214
short syndrome [NCBI] 0.000216043
RIEG1 [NCBI] 0.000172213
ophthalmoplegia, familial total, with iris transillumination [NCBI] 0.000143802
PITX2 [NCBI] 0.000127597
PPCD3 [NCBI] 0.000121332
heterochromia iridis [NCBI] 0.000112852
albinism, ocular, with sensorineural deafness [NCBI] 0.000112852
coloboma, ocular [NCBI] 9.11242e-05
WS2A [NCBI] 8.54328e-05
PPCD1 [NCBI] 8.12332e-05
TCF8 [NCBI] 7.57683e-05
COL18A1 [NCBI] 6.3916e-05
ZNF145 [NCBI] 5.42264e-05
WT1 [NCBI] 5.35619e-05
contractural arachnodactyly, congenital [NCBI] 5.2444e-05
SMS [NCBI] 5.23011e-05
TYR [NCBI] 4.63469e-05
MITF [NCBI] 4.4726e-05
NF1 [NCBI] 3.08316e-05
VRNI [NCBI] 2.02496e-05




Database Center for Life Science