MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Ichthyosiform Erythroderma, Congenital
[NCBI]
Gene
Gene
Link
Information
Gain
01
SPINK5
[NCBI]
0.000312358
NEWENTRY
[NCBI]
0.000240374
TGM1
[NCBI]
0.000112265
KRT1
[NCBI]
3.112e-05
ALOX12B
[NCBI]
2.69966e-05
NSDHL
[NCBI]
2.36961e-05
ABHD5
[NCBI]
2.22153e-05
KRT10
[NCBI]
1.78678e-05
NPAL2
[NCBI]
1.67592e-05
ICHTHYIN
[NCBI]
1.43788e-05
ALOXE3
[NCBI]
1.34804e-05
CYP4F22
[NCBI]
1.34804e-05
NIPA2
[NCBI]
1.2897e-05
LOR
[NCBI]
1.07066e-05
TGM3
[NCBI]
9.94342e-06
ABCA12
[NCBI]
9.62335e-06
ALOX12
[NCBI]
9.17627e-06
SCN9A
[NCBI]
7.97499e-06
IKBKG
[NCBI]
7.39169e-06
GJB2
[NCBI]
3.99012e-06
OMIM
OMIM
Link
Information
gain
01
NNCI
[NCBI]
0.00115589
LI5
[NCBI]
0.00107364
peeling skin syndrome
[NCBI]
0.000900049
LI1
[NCBI]
0.000824283
NCIE1
[NCBI]
0.000628042
NETH
[NCBI]
0.000492236
SPINK5
[NCBI]
0.000291873
LI3
[NCBI]
0.000218924
KRT10
[NCBI]
0.000210686
bullous erythroderma ichthyosiformis congenita of brocq
[NCBI]
0.000200717
TGM1
[NCBI]
0.000189154
ALOXE3
[NCBI]
0.000182473
congenital hemidysplasia with ichthyosiform erythroderma and limb defects
[NCBI]
0.000170839
CDS
[NCBI]
0.000168437
ALOX12B
[NCBI]
0.000163492
KRT1
[NCBI]
0.000121277
nevus, epidermal, epidermolytic hyperkeratotic type
[NCBI]
0.000100673
LI2
[NCBI]
9.1078e-05
vohwinkel syndrome, variant form
[NCBI]
8.78187e-05
gaucher disease, perinatal lethal
[NCBI]
7.73439e-05
ichthyin
[NCBI]
7.71252e-05
keratitis-ichthyosis-deafness syndrome, autosomal dominant
[NCBI]
6.90923e-05
NSDHL
[NCBI]
6.40367e-05
LOR
[NCBI]
5.97044e-05
EKV
[NCBI]
5.96288e-05
Database Center for Life Science