Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Hyperkeratosis, Epidermolytic [NCBI]

Gene


 Gene Link Information
Gain		 01
FRA12A [NCBI] 0.000499621
KRT10 [NCBI] 0.000384842
KRT1 [NCBI] 0.000308065
KRT2 [NCBI] 0.000135068
KRT9 [NCBI] 3.41031e-05
GJB4 [NCBI] 2.53755e-05
GJB3 [NCBI] 1.72915e-05
KRTAP5-1 [NCBI] 1.62697e-05
TGM5 [NCBI] 1.29909e-05
KRT6C [NCBI] 1.05167e-05
KRT6B [NCBI] 1.00853e-05
KRT6A [NCBI] 9.54474e-06
CTSC [NCBI] 8.57886e-06
KRIT1 [NCBI] 6.94483e-06
SFN [NCBI] 6.36859e-06
KRT5 [NCBI] 6.28456e-06
KRT14 [NCBI] 5.96229e-06
ERCC2 [NCBI] 4.35217e-06
MYC [NCBI] 3.93807e-06
GJB2 [NCBI] 3.52171e-06



OMIM


 OMIM Link Information
gain		 01
bullous erythroderma ichthyosiformis congenita of brocq [NCBI] 0.00442487
KRT1 [NCBI] 0.000686359
KRT2A [NCBI] 0.000371845
KRT10 [NCBI] 0.000365409
EKV [NCBI] 0.000294117
ichthyosis, cyclic, with epidermolytic hyperkeratosis [NCBI] 0.000243977
ichthyosis, bullous type [NCBI] 0.000171102
KRT9 [NCBI] 0.000114945
ichthyosis, hystrix-like, with deafness [NCBI] 9.93556e-05
KRT15 [NCBI] 8.71994e-05
mental retardation, fra12a type [NCBI] 7.80401e-05
HMS [NCBI] 7.30194e-05
GJB4 [NCBI] 6.23336e-05
PALS [NCBI] 5.68226e-05
EPS [NCBI] 5.60591e-05
KRIT1 [NCBI] 5.06988e-05
KRT5 [NCBI] 4.4001e-05
CTSC [NCBI] 4.33297e-05
LI1 [NCBI] 4.24691e-05
CCM [NCBI] 4.04259e-05
RASA1 [NCBI] 3.33977e-05
GJB2 [NCBI] 2.70181e-05



Database Center for Life Science