MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Dermatitis, Exfoliative
[NCBI]
Gene
Gene
Link
Information
Gain
01
KWE
[NCBI]
0.000438875
SPINK5
[NCBI]
5.01252e-05
TGM1
[NCBI]
3.26739e-05
GJB4
[NCBI]
1.36815e-05
LOR
[NCBI]
1.25575e-05
EBP
[NCBI]
1.09706e-05
KIR2DL2
[NCBI]
1.04566e-05
ALDH3A2
[NCBI]
9.87939e-06
GJB3
[NCBI]
9.7678e-06
PTPRC
[NCBI]
9.10436e-06
RAG2
[NCBI]
8.39443e-06
CCL17
[NCBI]
8.07524e-06
CCR4
[NCBI]
7.94019e-06
CXCR3
[NCBI]
6.74446e-06
RAG1
[NCBI]
6.65943e-06
GJB2
[NCBI]
5.79948e-06
OMIM
OMIM
Link
Information
gain
01
keratolytic winter erythema
[NCBI]
0.00200072
erythroderma, lethal congenital
[NCBI]
0.00119841
erythrokeratodermia variabilis 3
[NCBI]
0.000898321
trichohepatoenteric syndrome
[NCBI]
0.000844965
EKV
[NCBI]
0.000792262
complement component 5 deficiency
[NCBI]
0.000418878
NETH
[NCBI]
0.000164737
LOR
[NCBI]
0.00014762
erythrokeratodermia, progressive symmetric
[NCBI]
0.00013289
GJB3
[NCBI]
0.000126586
bullous erythroderma ichthyosiformis congenita of brocq
[NCBI]
0.000122444
ichthyosis, hystrix-like, with deafness
[NCBI]
0.000110422
ichthyosis, x-linked
[NCBI]
0.000101094
ichthyosis, bullous type
[NCBI]
8.40597e-05
kindler syndrome
[NCBI]
7.71411e-05
ichthyosis vulgaris
[NCBI]
7.33947e-05
CDS
[NCBI]
7.33947e-05
GJB4
[NCBI]
7.20115e-05
keratitis-ichthyosis-deafness syndrome, autosomal dominant
[NCBI]
7.03584e-05
omenn syndrome
[NCBI]
6.94617e-05
ichthyosis congenita, harlequin fetus type
[NCBI]
6.7806e-05
SPINK5
[NCBI]
6.26709e-05
CDPX2
[NCBI]
5.85232e-05
DKC
[NCBI]
5.72558e-05
TGM1
[NCBI]
5.69272e-05
LI1
[NCBI]
5.33212e-05
GJB2
[NCBI]
3.65463e-05
Database Center for Life Science