Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Lens Subluxation [NCBI]

Gene


 Gene Link Information
Gain		 01
FBN1 [NCBI] 4.16846e-05
SUOX [NCBI] 1.61034e-05



OMIM


 OMIM Link Information
gain		 01
ectopia lentis with ectopia of pupil [NCBI] 0.00102023
ectopia lentis [NCBI] 0.000246844
VRNI [NCBI] 0.000237353
molybdenum cofactor deficiency [NCBI] 0.000194088
blepharoptosis, myopia, and ectopia lentis [NCBI] 0.000145155
homocystinuria [NCBI] 0.000124421
epidermolysis bullosa, late-onset localized junctional, with mental retardation [NCBI] 0.000108698
weill-marchesani syndrome, autosomal dominant [NCBI] 0.000108698
sulfocysteinuria [NCBI] 9.86293e-05
ectopia lentis, isolated [NCBI] 9.63076e-05
wildervanck syndrome [NCBI] 8.93796e-05
RP [NCBI] 7.16244e-05
FBN1 [NCBI] 5.25921e-05
MFS [NCBI] 3.98448e-05



Database Center for Life Science