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MeSH keywords -> Related genes, diseases (OMIM)


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01 Ectopia Lentis [NCBI]


Gene


Gene Link Information
Gain
01
FBN1 [NCBI] 0.000143046
PAX6 [NCBI] 7.72918e-06
EGF [NCBI] 3.23145e-06




OMIM


OMIM Link Information
gain
01
ectopia lentis with ectopia of pupil [NCBI] 0.00354984
ectopia lentis, spontaneous filtering blebs, and craniofacial dysmorphism [NCBI] 0.00123814
ectopia lentis, isolated [NCBI] 0.000754853
MFS [NCBI] 0.000719224
FBN1 [NCBI] 0.000413729
ectopia lentis [NCBI] 0.000373356
craniosynostosis with ectopia lentis [NCBI] 0.000373356
homocystinuria [NCBI] 0.000145496
ectopia pupillae [NCBI] 0.00013578
blepharoptosis, myopia, and ectopia lentis [NCBI] 0.00013578
kniest-like dysplasia with pursed lips and ectopia lentis [NCBI] 0.000113311
contractural arachnodactyly, congenital [NCBI] 0.000109601
GEMSS [NCBI] 0.000104833
weill-marchesani syndrome, autosomal dominant [NCBI] 9.93282e-05
foveal hypoplasia and presenile cataract syndrome [NCBI] 8.92647e-05
PAX6 [NCBI] 4.27023e-05
EGF [NCBI] 3.56537e-06




Database Center for Life Science