Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Hyperkeratosis, Epidermolytic	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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