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MeSH keywords -> Related genes, diseases (OMIM)


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01 Blepharophimosis [NCBI]

Gene


 Gene Link Information
Gain		 01
FOXL2 [NCBI] 0.000591747
BPESC1 [NCBI] 0.000499621
SOX14 [NCBI] 5.10817e-05
TWIST1 [NCBI] 1.56292e-05
MRPS22 [NCBI] 1.31238e-05
ATR [NCBI] 1.28315e-05
RFC2 [NCBI] 1.10764e-05
SEPT9 [NCBI] 9.51898e-06
IRF6 [NCBI] 8.01651e-06
RPA1 [NCBI] 6.46938e-06
CKAP4 [NCBI] 5.60791e-06
TP63 [NCBI] 4.88732e-06



OMIM


 OMIM Link Information
gain		 01
BPES [NCBI] 0.00417117
mental retardation, congenital heart disease, blepharophimosis, blepharoptosis, and hypoplastic teeth [NCBI] 0.00310957
marden-walker syndrome [NCBI] 0.0025844
VDEGS [NCBI] 0.00251454
FOXL2 [NCBI] 0.00141149
blepharocheilodontic syndrome [NCBI] 0.00131194
dubowitz syndrome [NCBI] 0.000940744
blepharophimosis with ptosis, syndactyly, and short stature [NCBI] 0.000785962
kaufman oculocerebrofacial syndrome [NCBI] 0.000703952
corpus callosum, agenesis of, with facial anomalies and robin sequence [NCBI] 0.000553845
DURS1 [NCBI] 0.000419401
SOX14 [NCBI] 0.000265893
young-simpson syndrome [NCBI] 0.000182856
blepharophimosis with facial and genital anomalies and mental retardation [NCBI] 0.000125147
oculopalatoskeletal syndrome [NCBI] 8.87053e-05
GCS1 [NCBI] 8.46164e-05
MRPS22 [NCBI] 6.91455e-05
langer mesomelic dysplasia [NCBI] 6.68414e-05
SCS [NCBI] 4.77224e-05
ATR [NCBI] 4.77153e-05
TWIST1 [NCBI] 4.60244e-05



Database Center for Life Science